A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523136



Internal ID15450429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45698582..45866209hg38UCSC Ensembl
Innerchr15:45990780..46158407hg19UCSC Ensembl
Innerchr15:43778072..43945699hg18UCSC Ensembl
Innerchr15:43778072..43945699hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38167628
hg19167628
hg18167628
hg17167628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698841
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523136
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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