A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586479



Internal ID16373888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62143364..62144293hg38UCSC Ensembl
Innerchr20:60718420..60719349hg19UCSC Ensembl
Innerchr20:60151815..60152744hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38930
hg19930
hg18930
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7648n54
Supporting Variantsnssv942070, nssv942076, nssv942067, nssv942079, nssv942062, nssv942063, nssv942074, nssv942061, nssv942060, nssv942065, nssv942071, nssv942075, nssv942077, nssv942078, nssv942057, nssv942069, nssv942072, nssv942059, nssv942073, nssv942056, nssv942064, nssv942068, nssv942058, nssv942066
Samples
Known GenesPSMA7, SS18L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586479
Frequency
Sample Size17421
Observed Gain23
Observed Loss1
Observed Complex0
Frequencyn/a


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