A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569967



Internal ID16357376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73368274..73368898hg38UCSC Ensembl
Innerchr15:73660615..73661239hg19UCSC Ensembl
Innerchr15:71447668..71448292hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38625
hg19625
hg18625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845255
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569967
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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