A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569076



Internal ID16009799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34443896..34506266hg38UCSC Ensembl
Innerchr15:34736097..34798467hg19UCSC Ensembl
Innerchr15:32523389..32585759hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3862371
hg1962371
hg1862371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4472n54
Supporting Variantsnssv840287, nssv840286
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569076
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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