A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569956



Internal ID16357365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73367877..73368898hg38UCSC Ensembl
Innerchr15:73660218..73661239hg19UCSC Ensembl
Innerchr15:71447271..71448292hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381022
hg191022
hg181022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4619n54
Supporting Variantsnssv845231
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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