A curated catalogue of human genomic structural variation
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Keyword, Landmark or Region Search:
GRCh37/hg19
GRCh38/hg38
NCBI36/hg18
Examples:
RP11-34P13; CFTR, 7q11.21; chr7:71890181-72690180
Find DGV Variants
by Study
by Sample
by Method
by Variant
by Platform
by Chromosome
Summary Statistics
Stat
Merged-level
Sample-level
CNVs:
983845
7021692
Inversions:
4083
32044
Number of Studies:
75
News: February 2020 Update and Newsletter has been issued
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