A curated catalogue of human genomic structural variation




Keyword, Landmark or Region Search:

Examples: RP11-34P13; CFTR, 7q11.21; chr7:71890181-72690180


Find DGV Variants

by Studyby Sample
by Methodby Variant
by Platformby Chromosome

Summary Statistics

StatMerged-levelSample-level
CNVs:1098632304349
Inversions:2383380
Number of Studies:55


News: DGV will be unavailable this Monday, September 22nd from 10am to 12pm due to scheduled maintenance


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer