A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv845228



Internal ID16139184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73367751..73372400hg38UCSC Ensembl
Innerchr15:73660092..73664741hg19UCSC Ensembl
Innerchr15:71447145..71451794hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg384650
hg194650
hg184650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569954
Supporting Variants
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv845228
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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