A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567333



Internal ID16354742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20352819..20418387hg38UCSC Ensembl
Innerchr15:20558072..20623640hg19UCSC Ensembl
Innerchr15:18818086..18883654hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3865569
hg1965569
hg1865569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4184n54
Supporting Variantsnssv837130
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567333
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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