A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569062



Internal ID16009785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34506266hg38UCSC Ensembl
Innerchr15:34730758..34798467hg19UCSC Ensembl
Innerchr15:32518050..32585759hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3867710
hg1967710
hg1867710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4472n54
Supporting Variantsnssv840152, nssv840158, nssv840160, nssv840156, nssv840150, nssv840159, nssv840154, nssv840148, nssv840161, nssv840157, nssv840153, nssv840149, nssv840155, nssv840151
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569062
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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