Database of Genomic Variants
Also known as A curated catalogue of human genomic structural variation · DGV
The objective of the Database of Genomic Variants is to provide a comprehensive summary of structural variation in the human genome. We define structural variation as genomic alterations that involve segments of DNA that are larger than >1kb. Now we also annotate InDels in 100bp-1kb range. The content of the database is only representing structural variation identified in healthy control samples. The Database of Genomic Variants provides a useful catalog of control data for studies aiming to correlate genomic variation with phenotypic data. The database is continuously updated with new data from peer reviewed research studies. We always welcome suggestions and comments regarding the databas…
Getting access
Open access Open
- How to apply
- Not yet verified — we don’t publish a route we haven’t checked.
Summarised from a registry — the exact application route is not yet verified.
About this database
| Website | https://dgv.tcag.ca/dgv/app/home |
|---|---|
| Subjects | Life Sciences · Medicine · Medicine · Human Genetics |
| Last updated | 2026-09-11 |