A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569063



Internal ID16009786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34508394hg38UCSC Ensembl
Innerchr15:34730758..34800595hg19UCSC Ensembl
Innerchr15:32518050..32587887hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3869838
hg1969838
hg1869838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4472n54
Supporting Variantsnssv840174, nssv840177, nssv840170, nssv840164, nssv840168, nssv840171, nssv840165, nssv840173, nssv840163, nssv840166, nssv840162, nssv840175, nssv840169, nssv840172, nssv840167, nssv840176
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569063
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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