A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569965



Internal ID16357374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73368116..73368730hg38UCSC Ensembl
Innerchr15:73660457..73661071hg19UCSC Ensembl
Innerchr15:71447510..71448124hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38615
hg19615
hg18615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4622n54
Supporting Variantsnssv845252
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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