A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567318



Internal ID16354727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20299758..20428007hg38UCSC Ensembl
Innerchr15:20505011..20633260hg19UCSC Ensembl
Innerchr15:18765025..18893274hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38128250
hg19128250
hg18128250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4181n54
Supporting Variantsnssv837114
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567318
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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