A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567342



Internal ID16354751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20354526..20420780hg38UCSC Ensembl
Innerchr15:20559779..20626033hg19UCSC Ensembl
Innerchr15:18819793..18886047hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3866255
hg1966255
hg1866255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4188n54
Supporting Variantsnssv837139
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567342
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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