A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567434



Internal ID16354843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381928..20418387hg38UCSC Ensembl
Innerchr15:20587181..20623640hg19UCSC Ensembl
Innerchr15:18847195..18883654hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3836460
hg1936460
hg1836460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4198n54
Supporting Variantsnssv837261
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567434
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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