A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567335



Internal ID16354744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20352819..20421165hg38UCSC Ensembl
Innerchr15:20558072..20626418hg19UCSC Ensembl
Innerchr15:18818086..18886432hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3868347
hg1968347
hg1868347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4184n54
Supporting Variantsnssv837132
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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