A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569961



Internal ID16357370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73367998..73368782hg38UCSC Ensembl
Innerchr15:73660339..73661123hg19UCSC Ensembl
Innerchr15:71447392..71448176hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38785
hg19785
hg18785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4619n54
Supporting Variantsnssv845245
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569961
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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