A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694581



Internal ID15431233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35691554..35703284hg38UCSC Ensembl
Innerchr2:35916620..35928350hg19UCSC Ensembl
Innerchr2:35770124..35781854hg18UCSC Ensembl
Innerchr2:35828271..35840001hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3811731
hg1911731
hg1811731
hg1711731
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519867
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694581
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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