A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699651



Internal ID15436303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23913987..23916782hg38UCSC Ensembl
Innerchr13:24488126..24490921hg19UCSC Ensembl
Innerchr13:23386126..23388921hg18UCSC Ensembl
Innerchr13:23386126..23388921hg17UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg382796
hg192796
hg182796
hg172796
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523820
Supporting Variants
Samples
Known GenesANKRD20A19P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699651
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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