A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569954



Internal ID16357363
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 StatusM
Merged Variants
Supporting Variantsnssv845229, nssv845228
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569954
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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