A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837146



Internal ID16131102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20367552..20442400hg38UCSC Ensembl
Innerchr15:20572805..20647653hg19UCSC Ensembl
Innerchr15:18832819..18907667hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3874849
hg1974849
hg1874849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567349
Supporting Variants
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv837146
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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