is a Data Source.
The Database of Genomic Variants (DGV) provides a curated catalogue of structural variation in the genomes of control individuals from healthy populations. It compiles copy-number variants, insertions, deletions, inversions, and other structural variants reported in the literature to provide a reference for studies of genomic disorders.
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| ID | Name | URL | Category | Format | Description |
|---|---|---|---|---|---|
| dgv.site | DGV Web Interface | home | GraphicalInterface | http | Web interface for browsing and search... |
| dgv.downloads ⚠ | DGV Downloads | downloads | Product | mixed | Downloads of curated structural varia... |
| ID | Name | URL | Category | Format | Relation | Description |
|---|---|---|---|---|---|---|
| genecards.web.interface | GeneCards Web Interface | www.genecards.org | GraphicalInterface | http | had primary source | Web-based interface for searching and... |
| genomickb.graph | GenomicKB Graph Dump | genomickb-a-knowledgebase-for-the-human-genome | GraphProduct | http | had primary source | GenomicKB 1.0 Neo4j Database Dump (Re... |
The Database of Genomic Variants (DGV) is a curated collection of structural variation identified in the genomes of control individuals from healthy populations. Maintained by The Centre for Applied Genomics at The Hospital for Sick Children (Toronto), DGV serves as a reference for the interpretation of structural variants in clinical and research settings.
Content includes:
GeneCards integrates structural variation data from DGV.
Created: June 17, 2026 | Last modified: June 17, 2026