A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569963



Internal ID16357372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73368049..73368678hg38UCSC Ensembl
Innerchr15:73660390..73661019hg19UCSC Ensembl
Innerchr15:71447443..71448072hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38630
hg19630
hg18630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4622n54
Supporting Variantsnssv845248, nssv845249
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569963
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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