A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567324



Internal ID16354733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20334643..20420780hg38UCSC Ensembl
Innerchr15:20539896..20626033hg19UCSC Ensembl
Innerchr15:18799910..18886047hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3886138
hg1986138
hg1886138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4184n54
Supporting Variantsnssv837120
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567324
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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