A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659176



Internal ID15395828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35593041..35855307hg38UCSC Ensembl
Innerchr2:35818107..36080373hg19UCSC Ensembl
Innerchr2:35671611..35933877hg18UCSC Ensembl
Innerchr2:35729758..35992024hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38262267
hg19262267
hg18262267
hg17262267
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)nssv659176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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