A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569962



Internal ID16357371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73367998..73368898hg38UCSC Ensembl
Innerchr15:73660339..73661239hg19UCSC Ensembl
Innerchr15:71447392..71448292hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38901
hg19901
hg18901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4619n54
Supporting Variantsnssv845246, nssv845247
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569962
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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