A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698087



Internal ID15434739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72958144..72971064hg38UCSC Ensembl
Innerchr15:73250485..73263405hg19UCSC Ensembl
Innerchr15:71037538..71050458hg18UCSC Ensembl
Innerchr15:71037538..71050458hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3812921
hg1912921
hg1812921
hg1712921
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521475
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698087
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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