A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698129



Internal ID15434781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17727481..17749940hg38UCSC Ensembl
Innerchr11:17749028..17771487hg19UCSC Ensembl
Innerchr11:17705604..17728063hg18UCSC Ensembl
Innerchr11:17705604..17728063hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822460
hg1922460
hg1822460
hg1722460
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521511
Supporting Variants
Samples
Known GenesKCNC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698129
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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