Resource

Id hg38/scores/ClinVar_20261011content_copy
Type allele_score
Version 0
Summary Measure used to assess the clinical significance of genetic variants
Description
Labels
  • reference_genome: hg38/genomes/ucsc-hg38

Scores (27)

ID Type Default annotation Description Histogram Range Summary
AF_ESP float

-

allele frequencies from GO-ESP
Small values desc: low frequency
Large values desc: high frequency
HISTOGRAM FOR AF_ESP [8e-05, 1]
n
412,060
mean
0.0226
sd
0.104
AF_EXAC float

-

allele frequencies from ExAC
Small values desc: low frequency
Large values desc: high frequency
HISTOGRAM FOR AF_EXAC [0, 1]
n
953,294
mean
0.00916
sd
0.0688
AF_TGP float

-

allele frequencies from TGP
Small values desc: low frequency
Large values desc: high frequency
HISTOGRAM FOR AF_TGP [0, 1]
n
445,655
mean
0.0622
sd
0.169
ALLELEID int

-

ClinVar Allele ID
HISTOGRAM FOR ALLELEID [1.5e+04, 5.13e+06]
n
4,594,763
mean
2.67e+06
sd
1.47e+06
CLNDN str

CLNDN

ClinVar's preferred disease name for the concept specified by disease identifiers in CLNDISDB
HISTOGRAM FOR CLNDN not_specified, not_provided, Inborn_genetic_diseases, Hereditary_cancer-predisposing_syndrome, not_specified|not_provided, Cardiovascular_phenotype, not_provided|not_specified, Inborn_genetic_diseases|not_provided, not_provided|Inborn_genetic_diseases, Primary_ciliary_dyskinesia (top 10 of 230956 values)
CLNDNINCL str

-

For included Variant : ClinVar's preferred disease name for the concept specified by disease identifiers in CLNDISDB
HISTOGRAM FOR CLNDNINCL not_specified, Vancomycin_response, Leber_congenital_amaurosis, Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency, Cystic_fibrosis, not_provided, Citalopram_response|Escitalopram_response|Sertraline_response|Voriconazole_response, Abnormality_of_neuronal_migration, Acyl-CoA_dehydrogenase_9_deficiency, 21-Hydroxylase-Deficient_Congenital_Adrenal_Hyperplasia, Severe_early-childhood-onset_retinal_dystrophy, Vici_syndrome, Hypercholesterolemia|_familial|_1, Opsismodysplasia, Alpha-1-antitrypsin_deficiency, Familial_hypokalemia-hypomagnesemia, Autosomal_recessive_nonsyndromic_hearing_loss_3, Breast-ovarian_cancer|_familial|_susceptibility_to|_1, Reclassified_-_variant_of_unknown_significance, Fabry_disease (top 20 of 642 values)
CLNDISDB str

-

Tag-value pairs of disease database name and identifier submitted for germline classifications, e.g. OMIM:NNNNNN"
HISTOGRAM FOR CLNDISDB MedGen:CN169374, MedGen:C3661900, MeSH:D030342|MedGen:C0950123, ., MONDO:MONDO:0015356|MeSH:D009386|MedGen:C0027672|Orphanet:140162, MedGen:CN169374|MedGen:C3661900, MedGen:CN230736, MedGen:C3661900|MedGen:CN169374, MeSH:D030342|MedGen:C0950123|MedGen:C3661900, MedGen:C3661900|MeSH:D030342|MedGen:C0950123, .|MedGen:C3661900, Human_Phenotype_Ontology:HP:0012265|MONDO:MONDO:0016575|MedGen:C0008780|OMIM:PS244400|Orphanet:244, MedGen:C3661900|., MedGen:CN517202, MONDO:MONDO:0800491|MedGen:C0393706|Orphanet:1934, MONDO:MONDO:0019391|MeSH:D005199|MedGen:C0015625|OMIM:PS227650|Orphanet:84, MONDO:MONDO:0011400|MedGen:C1858763|OMIM:604145|Orphanet:154|MONDO:MONDO:0012127|MedGen:C1837342|OMIM:608807|Orphanet:140922, MONDO:MONDO:0009725|MedGen:C1850569|OMIM:256030, Human_Phenotype_Ontology:HP:0001258|Human_Phenotype_Ontology:HP:0007062|Human_Phenotype_Ontology:HP:0007124|Human_Phenotype_Ontology:HP:0007216|MedGen:C0037772, MONDO:MONDO:0019625|MedGen:C4707243|OMIM:PS607086|Orphanet:91387 (top 20 of 198267 values)
CLNDISDBINCL str

-

For included Variant: Tag-value pairs of disease database name and identifier for germline classifications, e.g. OMIM:NNNNNN
HISTOGRAM FOR CLNDISDBINCL ., MedGen:CN169374, MedGen:CN297638, MONDO:MONDO:0018998|MeSH:D057130|MedGen:C0339527|OMIM:PS204000|Orphanet:65, MONDO:MONDO:0010480|MedGen:C2720289|OMIM:300908|Orphanet:466026, MONDO:MONDO:0009061|MedGen:C0010674|OMIM:219700|Orphanet:586, MedGen:C3661900, MedGen:CN221263|MedGen:CN221264|MedGen:CN221265|MedGen:CN077957, Human_Phenotype_Ontology:HP:0002269|Human_Phenotype_Ontology:HP:0007317|MedGen:C1837249, MONDO:MONDO:0012624|MedGen:C4747517|OMIM:611126|Orphanet:99901, MedGen:C2936858|OMIM:201910, MONDO:MONDO:0009549|MeSH:D000080362|MedGen:C1855465|OMIM:248200|Orphanet:364055|Orphanet:827, MONDO:MONDO:0009452|MedGen:C1855772|OMIM:242840|Orphanet:1493, .|., .|MedGen:CN221263|MedGen:CN221264|MedGen:CN221265|MedGen:CN077957, MONDO:MONDO:0007750|MedGen:C0745103|OMIM:143890|Orphanet:391665, MONDO:MONDO:0009785|MedGen:C0432219|OMIM:258480|Orphanet:2746, MONDO:MONDO:0013282|MedGen:C0221757|OMIM:613490|Orphanet:60, MONDO:MONDO:0009904|MedGen:C0268450|OMIM:263800|Orphanet:358, MONDO:MONDO:0010860|MedGen:C1838263|OMIM:600316|Orphanet:90636 (top 20 of 580 values)
CLNREVSTAT str

-

ClinVar review status of germline classification for the Variation ID
HISTOGRAM FOR CLNREVSTAT criteria_provided|_single_submitter, criteria_provided|_multiple_submitters|_no_conflicts, criteria_provided|_conflicting_classifications, no_assertion_criteria_provided, reviewed_by_expert_panel, no_classification_provided, no_classification_for_the_single_variant, no_classifications_from_unflagged_records, practice_guideline
CLNSIG str

CLNSIG

Aggregate germline classification for this single variant; multiple values are separated by a vertical bar
HISTOGRAM FOR CLNSIG Uncertain_significance, Likely_benign, Benign, Pathogenic, Conflicting_classifications_of_pathogenicity, Likely_pathogenic, Benign/Likely_benign, Pathogenic/Likely_pathogenic, not_provided, drug_response, other, no_classification_for_the_single_variant, risk_factor, association, Uncertain_significance/Uncertain_risk_allele, no_classifications_from_unflagged_records, Affects, Likely_risk_allele, Pathogenic|_low_penetrance, Pathogenic|other (top 20 of 104 values)
CLNSIGCONF str

-

Conflicting germline classification for this single variant; multiple values are separated by a vertical bar
HISTOGRAM FOR CLNSIGCONF Uncertain_significance_(1)|Likely_benign_(1), Uncertain_significance_(2)|Likely_benign_(1), Uncertain_significance_(1)|Likely_benign_(2), Likely_pathogenic_(1)|Uncertain_significance_(1), Uncertain_significance_(3)|Likely_benign_(1), Uncertain_significance_(1)|Benign_(1), Uncertain_significance_(4)|Likely_benign_(1), Uncertain_significance_(1)|Likely_benign_(3), Uncertain_significance_(2)|Likely_benign_(2), Pathogenic_(1)|Uncertain_significance_(1), Uncertain_significance_(1)|Benign_(1)|Likely_benign_(1), Likely_pathogenic_(1)|Uncertain_significance_(2), Uncertain_significance_(5)|Likely_benign_(1), Uncertain_significance_(2)|Benign_(1), Uncertain_significance_(3)|Likely_benign_(2), Uncertain_significance_(1)|Benign_(1)|Likely_benign_(2), Uncertain_significance_(1)|Likely_benign_(4), Likely_pathogenic_(2)|Uncertain_significance_(1), Uncertain_significance_(2)|Likely_benign_(3), Uncertain_significance_(6)|Likely_benign_(1) (top 20 of 2250 values)
CLNSIGINCL str

-

Germline classification for a haplotype or genotype that includes this variant. Reported as pairs of VariationID:classification; multiple values are separated by a vertical bar
HISTOGRAM FOR CLNSIGINCL 1723892:drug_response, 14353:Uncertain_significance, 5345:Benign, 440728:risk_factor, 869112:association, 1184302:Uncertain_significance, 1022:risk_factor, 17709:Benign, 36924:Pathogenic, 29691:risk_factor, 4075782:Pathogenic, 12182:Pathogenic, 13542:risk_factor, 17736:Affects|2573152:Benign|2573153:Benign|2573154:Benign, 633844:drug_response|633885:drug_response|633887:drug_response|633888:drug_response|633904:drug_response|633905:drug_response|633910:drug_response|633913:drug_response|633916:drug_response|633925:drug_response|633927:drug_response|633930:drug_response|633941:drug_response|633952:drug_response|633958:drug_response|633965:drug_response|634060:drug_response|634114:drug_response|634132:drug_response|634136:drug_response|634137:drug_response|634138:drug_response|634205:drug_response|634212:drug_response|634213:drug_response|634232:drug_response|634272:drug_response|634298:drug_response|634355:drug_response|634365:drug_response|634375:drug_response|634413:drug_response|634414:drug_response|634427:drug_response|638789:drug_response, 438264:Pathogenic, 1722723:Likely_pathogenic, 202166:not_provided, 12304:Pathogenic, 14182:Pathogenic (top 20 of 1005 values)
CLNVC str

-

Variant type
HISTOGRAM FOR CLNVC single_nucleotide_variant, Deletion, Duplication, Microsatellite, Indel, Insertion, Inversion, Variation
CLNVCSO str

-

Sequence Ontology id for variant type
HISTOGRAM FOR CLNVCSO SO:0001483, SO:0000159, SO:1000035, SO:0000289, SO:1000032, SO:0000667, SO:1000036, SO:0001059
CLNVI str

-

the variant's clinical sources reported as tag-value pairs of database and variant identifier
HISTOGRAM FOR CLNVI OMIM:154270.0001, Genetic_Testing_Registry_(GTR):GTR000619748|Genetic_Testing_Registry_(GTR):GTR000619755|Genetic_Testing_Registry_(GTR):GTR000619758|Genetic_Testing_Registry_(GTR):GTR000619762, Genetic_Testing_Registry_(GTR):GTR000569522|Genetic_Testing_Registry_(GTR):GTR000613418, OMIM:111700.0002, OMIM:131230.0001, OMIM:610665.0001, OMIM:605634.0002, OMIM:152200.0002, Genetic_Testing_Registry_(GTR):GTR000569522|Genetic_Testing_Registry_(GTR):GTR000613302|Genetic_Testing_Registry_(GTR):GTR000613428, OMIM:611409.0013, OMIM:601146.0012, OMIM:611082.0001, OMIM:608515.0002, OMIM:102610.0015, OMIM:605556.0005, OMIM:146929.0001, OMIM:604083.0004, OMIM:601470.0001, OMIM:191328.0003, OMIM:607607.0003 (top 20 of 2884029 values)
GENEINFO str

-

Gene(s) for the variant reported as gene symbol:gene id. The gene symbol and id are delimited by a colon (:) and each pair is delimited by a vertical bar (|)
HISTOGRAM FOR GENEINFO BRCA2:675, TTN:7273|TTN-AS1:100506866, NF1:4763, APC:324, TTN:7273, BRCA1:672, TSC2:7249, ATM:472, POLE:5426, RYR1:6261, DMD:1756, MSH6:2956, NEB:4703, RYR2:6262, FBN1:2200, USH2A:7399, MSH2:4436, DICER1:23405, KMT2D:8085, ADGRV1:84059 (top 20 of 32314 values)
MC str

-

comma separated list of molecular consequence in the form of Sequence Ontology ID|molecular_consequence
HISTOGRAM FOR MC SO:0001583|missense_variant, SO:0001627|intron_variant, SO:0001819|synonymous_variant, SO:0001583|missense_variant|SO:0001619|non-coding_transcript_variant, SO:0001583|missense_variant|SO:0001627|intron_variant, SO:0001589|frameshift_variant, SO:0001619|non-coding_transcript_variant|SO:0001819|synonymous_variant, SO:0001587|nonsense, SO:0001624|3_prime_UTR_variant, SO:0001575|splice_donor_variant, SO:0001627|intron_variant|SO:0001819|synonymous_variant, SO:0001583|missense_variant|SO:0001623|5_prime_UTR_variant, SO:0001574|splice_acceptor_variant, SO:0001583|missense_variant|SO:0001619|non-coding_transcript_variant|SO:0001627|intron_variant, SO:0001583|missense_variant|SO:0001624|3_prime_UTR_variant, SO:0001583|missense_variant|SO:0001619|non-coding_transcript_variant|SO:0001623|5_prime_UTR_variant, SO:0001589|frameshift_variant|SO:0001619|non-coding_transcript_variant, SO:0001623|5_prime_UTR_variant, SO:0001623|5_prime_UTR_variant|SO:0001819|synonymous_variant, SO:0001822|inframe_deletion (top 20 of 696 values)
ONCDN str

-

ClinVar's preferred disease name for the concept specified by disease identifiers in ONCDISDB
HISTOGRAM FOR ONCDN Neoplasm, Meningioma, Gastrointestinal_stromal_tumor, Acute_myeloid_leukemia, Adenoid_cystic_carcinoma, Neuroendocrine_tumor_of_pancreas, Adrenal_cortex_carcinoma, Pineoblastoma, Colorectal_cancer, Chronic_myeloid_leukemia, Pancreatic_ductal_adenocarcinoma, Glioblastoma_multiforme|_somatic, Neoplasm|Meningioma, Cavernous_sinus_meningioma, Neoplasm|Colorectal_cancer, Squamous_cell_carcinoma_of_the_head_and_neck, Inflammatory_myofibroblastic_tumor_of_the_urinary_bladder, Adenoid_cystic_carcinoma|Neoplasm, Vulvar_adenocarcinoma_of_mammary_gland_type|Neoplasm, Lynch_syndrome, Other
ONCREVSTAT str

-

ClinVar review status of oncogenicity classification for the Variation ID
HISTOGRAM FOR ONCREVSTAT criteria_provided|_single_submitter, no_classification_for_the_single_variant, no_assertion_criteria_provided, criteria_provided|_multiple_submitters|_no_conflicts, criteria_provided|_conflicting_classifications
ONCDISDB str

-

Tag-value pairs of disease database name and identifier submitted for oncogenicity classifications, e.g. MedGen:NNNNNN
HISTOGRAM FOR ONCDISDB Human_Phenotype_Ontology:HP:0002664|Human_Phenotype_Ontology:HP:0003008|Human_Phenotype_Ontology:HP:0006741|MONDO:MONDO:0005070|MeSH:D009369|MedGen:C0027651, Human_Phenotype_Ontology:HP:0002858|Human_Phenotype_Ontology:HP:0006754|MONDO:MONDO:0016642|MedGen:C0025286|Orphanet:2495, Human_Phenotype_Ontology:HP:0100723|MONDO:MONDO:0011719|MeSH:D046152|MedGen:C0238198|OMIM:606764|Orphanet:44890, Human_Phenotype_Ontology:HP:0001914|Human_Phenotype_Ontology:HP:0004808|Human_Phenotype_Ontology:HP:0004843|Human_Phenotype_Ontology:HP:0005516|Human_Phenotype_Ontology:HP:0006724|Human_Phenotype_Ontology:HP:0006728|MONDO:MONDO:0018874|MeSH:D015470|MedGen:C0023467|OMIM:601626|Orphanet:519, MONDO:MONDO:0004971|MeSH:D003528|MedGen:C0010606, MONDO:MONDO:0019954|MedGen:C1337011|Orphanet:97253, Human_Phenotype_Ontology:HP:0002889|Human_Phenotype_Ontology:HP:0006744|Human_Phenotype_Ontology:HP:0006759|MONDO:MONDO:0006639|MeSH:D018268|MedGen:C0206686|Orphanet:1501, Human_Phenotype_Ontology:HP:0030408|Human_Phenotype_Ontology:HP:0040193|MONDO:MONDO:0016722|MedGen:C0205898|Orphanet:251909, MONDO:MONDO:0005575|MedGen:C0346629|OMIM:114500, Human_Phenotype_Ontology:HP:0005506|Human_Phenotype_Ontology:HP:0005544|MONDO:MONDO:0011996|MeSH:D015464|MedGen:C0279543|OMIM:608232|Orphanet:521, MONDO:MONDO:0005184|MedGen:C1335302, MedGen:C4016231, Human_Phenotype_Ontology:HP:0002664|Human_Phenotype_Ontology:HP:0003008|Human_Phenotype_Ontology:HP:0006741|MONDO:MONDO:0005070|MeSH:D009369|MedGen:C0027651|Human_Phenotype_Ontology:HP:0002858|Human_Phenotype_Ontology:HP:0006754|MONDO:MONDO:0016642|MedGen:C0025286|Orphanet:2495, MONDO:MONDO:0002996|MedGen:C1332865, Human_Phenotype_Ontology:HP:0002664|Human_Phenotype_Ontology:HP:0003008|Human_Phenotype_Ontology:HP:0006741|MONDO:MONDO:0005070|MeSH:D009369|MedGen:C0027651|MONDO:MONDO:0005575|MedGen:C0346629|OMIM:114500, Human_Phenotype_Ontology:HP:0020357|MONDO:MONDO:0010150|MeSH:D000077195|MedGen:C1168401|OMIM:275355|Orphanet:67037, ., MONDO:MONDO:0004971|MeSH:D003528|MedGen:C0010606|Human_Phenotype_Ontology:HP:0002664|Human_Phenotype_Ontology:HP:0003008|Human_Phenotype_Ontology:HP:0006741|MONDO:MONDO:0005070|MeSH:D009369|MedGen:C0027651, MedGen:C3839330|Human_Phenotype_Ontology:HP:0002664|Human_Phenotype_Ontology:HP:0003008|Human_Phenotype_Ontology:HP:0006741|MONDO:MONDO:0005070|MeSH:D009369|MedGen:C0027651, MONDO:MONDO:0005835|MedGen:C4552100|Orphanet:144, Other
ONC str

-

Aggregate oncogenicity classification for this single variant; multiple values are separated by a vertical bar
HISTOGRAM FOR ONC Likely_oncogenic, no_classification_for_the_single_variant, Uncertain_significance, Oncogenic, Likely_benign, Benign, Conflicting_classifications_of_oncogenicity
ORIGIN str

-

Allele origin
HISTOGRAM FOR ORIGIN 1, 0, 32, 33, 5, 2, 17, 4, 16, 9, 3, 8, 65, 64, 25, 21, 13, 35, 49, 37, Other
RS str

-

Gene(s) for the variant reported as gene symbol:gene id. The gene symbol and id are delimited by a colon (:) and each pair is delimited by a vertical bar (|)

No histogram: Histogram is not available for this score.

NO DOMAIN
SCIDN str

-

ClinVar's preferred disease name for the concept specified by disease identifiers in SCIDISDB
HISTOGRAM FOR SCIDN Embryonal_rhabdomyosarcoma, Diffuse_midline_glioma|_H3_K27M-mutant, Medulloblastoma_WNT_activated, Primary_central_nervous_system_lymphoma, Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype, Diffuse_glioma|_H3_G34_mutant, Neuroblastoma, Familial_cancer_of_breast, Pilocytic_astrocytoma, Medulloblastoma_non-WNT/non-SHH_group_3, Colorectal_cancer, Rhabdomyosarcoma, Germinoma, Medulloblastoma_non-WNT/non-SHH_group_4, Medulloblastoma_SHH_activated, Astrocytoma_IDH-mutant, Chronic_myeloid_leukemia, Medulloblastoma_SHH_activated_and_TP53_wild-type, Acute_myeloid_leukemia, Melanoma (top 20 of 313 values)
SCIDISDB str

-

Tag-value pairs of disease database name and identifier submitted for somatic clinial impact classifications, e.g. MedGen:NNNNNN
HISTOGRAM FOR SCIDISDB Human_Phenotype_Ontology:HP:0006743|MONDO:MONDO:0009993|MedGen:C0206656|Orphanet:99757, MONDO:MONDO:0957196|MedGen:C4289688, MONDO:MONDO:0850196|MedGen:C4331965, Human_Phenotype_Ontology:HP:0030069|MONDO:MONDO:0002571|MedGen:C0280803|Orphanet:46135, MONDO:MONDO:0858939|MedGen:C5669918, MONDO:MONDO:0957197|MedGen:CN377580, Human_Phenotype_Ontology:HP:0003006|Human_Phenotype_Ontology:HP:0006738|MONDO:MONDO:0005072|MeSH:D009447|MedGen:C0027819|Orphanet:635, MONDO:MONDO:0016419|MedGen:C0346153|OMIM:114480|Orphanet:227535, Human_Phenotype_Ontology:HP:0033680|MONDO:MONDO:0016691|MedGen:C0334583|Orphanet:251612, MONDO:MONDO:0956966|MedGen:C4330665, MONDO:MONDO:0005575|MedGen:C0346629|OMIM:114500, Human_Phenotype_Ontology:HP:0002859|MONDO:MONDO:0005212|MeSH:D012208|MedGen:C0035412|Orphanet:780, Human_Phenotype_Ontology:HP:0100620|MONDO:MONDO:0002598|MedGen:C0206660, MONDO:MONDO:0956967|MedGen:C4330666, MONDO:MONDO:0850197|MedGen:C4330671, MedGen:C5669733, Human_Phenotype_Ontology:HP:0005506|Human_Phenotype_Ontology:HP:0005544|MONDO:MONDO:0011996|MeSH:D015464|MedGen:C0279543|OMIM:608232|Orphanet:521, MONDO:MONDO:0956965|MedGen:CN377554, Human_Phenotype_Ontology:HP:0001914|Human_Phenotype_Ontology:HP:0004808|Human_Phenotype_Ontology:HP:0004843|Human_Phenotype_Ontology:HP:0005516|Human_Phenotype_Ontology:HP:0006724|Human_Phenotype_Ontology:HP:0006728|MONDO:MONDO:0018874|MeSH:D015470|MedGen:C0023467|OMIM:601626|Orphanet:519, Human_Phenotype_Ontology:HP:0002861|Human_Phenotype_Ontology:HP:0002887|Human_Phenotype_Ontology:HP:0006777|Human_Phenotype_Ontology:HP:0007474|MONDO:MONDO:0005105|MeSH:D008545|MedGen:C0025202 (top 20 of 312 values)
SCI str

-

Aggregate somatic clinical impact for this single variant; multiple values are separated by a vertical bar
HISTOGRAM FOR SCI Tier_I_-_Strong, no_classification_for_the_single_variant, Tier_II_-_Potential, Tier_III_-_Unknown, Tier_IV_-_Benign/Likely_benign
SCIREVSTAT str

-

ClinVar review status of somatic clinical impact for the Variation ID
HISTOGRAM FOR SCIREVSTAT criteria_provided|_single_submitter, no_classification_for_the_single_variant, no_assertion_criteria_provided, criteria_provided|_multiple_submitters

n counts alleles; sd is the population standard deviation.

Alleles

Chromosome Alleles substitution % insertion % deletion % complex % other %
all chromosomes 4594763 92.84% 2.17% 4.46% 0.49% 0.04%
chr1 414874 93.90% 1.76% 3.89% 0.40% 0.05%
chr2 401293 91.88% 2.47% 5.08% 0.53% 0.04%
chr3 251455 93.37% 2.00% 4.13% 0.46% 0.04%
chr4 163638 93.71% 1.88% 3.98% 0.41% 0.03%
chr5 222382 92.30% 2.43% 4.63% 0.60% 0.04%
chr6 206652 92.71% 2.16% 4.61% 0.48% 0.04%
chr6_GL000251v2_alt 1 100.00% 0.00% 0.00% 0.00% 0.00%
chr7 223271 93.27% 2.04% 4.17% 0.48% 0.04%
chr8 155590 93.09% 1.98% 4.46% 0.43% 0.05%
chr8_KI270821v1_alt 1 100.00% 0.00% 0.00% 0.00% 0.00%
chr9 203288 93.12% 2.26% 4.09% 0.48% 0.04%
chr10 171779 92.95% 2.28% 4.26% 0.46% 0.05%
chr11 267878 92.79% 2.14% 4.50% 0.53% 0.04%
chr12 211635 93.34% 1.96% 4.23% 0.43% 0.04%
chr13 90267 88.32% 3.41% 7.42% 0.78% 0.07%
chr14 145498 93.67% 1.92% 3.98% 0.40% 0.03%
chr15 159373 92.56% 2.26% 4.65% 0.47% 0.05%
chr16 237273 92.75% 2.18% 4.50% 0.55% 0.03%
chr17 277204 90.81% 2.72% 5.75% 0.66% 0.06%
chr17_KI270909v1_alt 11 100.00% 0.00% 0.00% 0.00% 0.00%
chr18 76648 93.23% 2.22% 4.12% 0.39% 0.04%
chr19 261627 94.68% 1.68% 3.18% 0.42% 0.04%
chr19_KI270938v1_alt 16 100.00% 0.00% 0.00% 0.00% 0.00%
chr20 99410 94.51% 1.70% 3.39% 0.37% 0.04%
chr21 51690 92.76% 2.36% 4.36% 0.46% 0.05%
chr22 99461 92.93% 2.07% 4.44% 0.50% 0.06%
chr22_KI270879v1_alt 20 100.00% 0.00% 0.00% 0.00% 0.00%
chrM 3135 96.14% 1.47% 2.11% 0.26% 0.03%
chrUn_GL000218v1 1 100.00% 0.00% 0.00% 0.00% 0.00%
chrX 198694 91.41% 2.60% 5.45% 0.46% 0.07%
chrY 698 95.70% 1.58% 2.58% 0.00% 0.14%

Substitution matrix

ref → alt A C G T
A0
0.00%
144596
3.39%
458976
10.76%
127495
2.99%
C258917
6.07%
0
0.00%
266357
6.24%
882814
20.70%
G880473
20.64%
264598
6.20%
0
0.00%
258189
6.05%
T125335
2.94%
454269
10.65%
143597
3.37%
0
0.00%
ts/tv
1.68
2,676,532 transitions / 1,589,084 transversions

Indel lengths

alleles min max mean median
insertions 99687 1 9970 13.64 1
deletions 205091 1 9982 36.46 2
insertion length histogram deletion length histogram

Complex alleles

complex allele length grid

Files

Filename Size md5
clinvar_20261011.vcf.gz 191.15 MB 0f3a1a5e84252386033d5fcab1bf1f6a
clinvar_20261011_chr.header.vcf.gz 1.3 KB 227bb0f3b4fb6c684c34cc17447e1652
clinvar_20261011_chr.vcf.gz 191.58 MB efbf67ab6fb53157234949825b7b46d1
clinvar_20261011_chr.vcf.gz.tbi 597.94 KB ac7296b511ef7f5f54fa99338e21622f
customplot1.py 8.09 KB 1482621843828d22ef8255a334a50e0f
dataprep.sh 2.55 KB 5b97f9295e4744d420a7ad7cdc515091
genomic_resource.yaml 10.26 KB acce1f933448ce62ea4e823d53b80adf
hg38.chromAlias.txt 26.65 KB 889533482362d1c7d2976e12d8367737
statistics/