A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567326



Internal ID16354735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20339825..20428007hg38UCSC Ensembl
Innerchr15:20545078..20633260hg19UCSC Ensembl
Innerchr15:18805092..18893274hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3888183
hg1988183
hg1888183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4184n54
Supporting Variantsnssv837122, nssv837123
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567326
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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