| Id: | hg38/cnv_collections/DGV |
| Type: | cnv_collection |
| Version: | 0 |
| Summary: |
Database of Genomic Variants (DGV) CNV collection |
| Description: |
The Database of Genomic Variants (DGV) is a curated resource that provides publicly available data on structural variation (e.g., deletions, duplications, insertions) in the human genome, collected from peer-reviewed studies. It serves as a key reference for understanding genomic variation in healthy individuals and distinguishing benign variants from disease-associated changes. Downloaded on 12/16/2024 from https://dgv.tcag.ca/dgv/docs/GRCh38_hg38_variants_2020-02-25.txt DataPrep.py converts raw file to GRR format. |
| Labels: |
| Filename | Size | md5 |
|---|---|---|
| DataPrep.py | 681.0 B | 5046dfa84795f7f2b22720161a04c745 |
| GRCh38_hg38_variants_2020-02-25.txt | 208.69 MB | 9a9267b3bd5889e97751ef1dec097ac0 |
| GRCh38_hg38_variants_2020-02-25.txt.dvc | 120.0 B | a605f936bdf9856b6c59745968ac9465 |
| genomic_resource.yaml | 1.02 KB | c39c73aa6b703b0f83814b656e04f125 |
| prepped_GRCh38_hg38_variants_2020-02-25.txt | 205.89 MB | 2ae47a5fb27037bc235d64a2faca7ec0 |
| prepped_GRCh38_hg38_variants_2020-02-25.txt.dvc | 128.0 B | f07ae9e09c984fdf62cf138e079d6068 |
| statistics/ |