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:9838457021692
Inversions:408332044
Number of Studies:75


News: May 2016 Update and Newsletter has been issued


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