A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567399



Internal ID16354808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20377603..20418203hg38UCSC Ensembl
Innerchr15:20582856..20623456hg19UCSC Ensembl
Innerchr15:18842870..18883470hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3840601
hg1940601
hg1840601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4198n54
Supporting Variantsnssv837217
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567399
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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