A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569226



Internal ID16356635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39452224..39455957hg38UCSC Ensembl
Innerchr15:39744425..39748158hg19UCSC Ensembl
Innerchr15:37531717..37535450hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383734
hg193734
hg183734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4498n54
Supporting Variantsnssv842218, nssv842214, nssv842207, nssv842202, nssv842197, nssv842213, nssv842200, nssv842206, nssv842212, nssv842209, nssv842211, nssv842216, nssv842204, nssv842198, nssv842208, nssv842205, nssv842210, nssv842201, nssv842199, nssv842217, nssv842215, nssv842203
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569226
Frequency
Sample Size17421
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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