A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839656



Internal ID16133612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31484140..31494905hg38UCSC Ensembl
Innerchr15:31776343..31787108hg19UCSC Ensembl
Innerchr15:29563635..29574400hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3810766
hg1910766
hg1810766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568824
Supporting Variants
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839656
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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