A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569957



Internal ID16357366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73367928..73368782hg38UCSC Ensembl
Innerchr15:73660269..73661123hg19UCSC Ensembl
Innerchr15:71447322..71448176hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38855
hg19855
hg18855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4620n54
Supporting Variantsnssv845232
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569957
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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