A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567464



Internal ID16354873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20405959..20420780hg38UCSC Ensembl
Innerchr15:20611212..20626033hg19UCSC Ensembl
Innerchr15:18871226..18886047hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3814822
hg1914822
hg1814822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv837297
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567464
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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