A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569953



Internal ID16357362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73367751..73368898hg38UCSC Ensembl
Innerchr15:73660092..73661239hg19UCSC Ensembl
Innerchr15:71447145..71448292hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381148
hg191148
hg181148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4620n54
Supporting Variantsnssv845222, nssv845220, nssv845218, nssv845226, nssv845227, nssv845225, nssv845219, nssv845224, nssv845221, nssv845223
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569953
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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