A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526683



Internal ID15107290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236143831..236165133hg38UCSC Ensembl
Innerchr2:237052475..237073776hg19UCSC Ensembl
Innerchr2:236717214..236738515hg18UCSC Ensembl
Innerchr2:236834475..236855776hg17UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3821303
hg1921302
hg1821302
hg1721302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703015
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526683
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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