A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569442



Internal ID16010165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53598196..54164557hg38UCSC Ensembl
Innerchr15:53890393..54456754hg19UCSC Ensembl
Innerchr15:51677685..52244046hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38566362
hg19566362
hg18566362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4531n54
Supporting Variantsnssv1148870
SamplesHGDP00130
Known GenesUNC13C, WDR72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569442
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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