A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585258



Internal ID16372667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1914433..1914987hg38UCSC Ensembl
Innerchr20:1895079..1895633hg19UCSC Ensembl
Innerchr20:1843079..1843633hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38555
hg19555
hg18555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937240, nssv937245, nssv937244, nssv937247, nssv937262, nssv937238, nssv937260, nssv937256, nssv937252, nssv937249, nssv937250, nssv937263, nssv937258, nssv937255, nssv937242, nssv937239, nssv937268, nssv937241, nssv937261, nssv937243, nssv937259, nssv937254, nssv937265, nssv937246, nssv937266, nssv937267, nssv937264, nssv937251, nssv937257, nssv937248, nssv937253
Samples
Known GenesSIRPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585258
Frequency
Sample Size17421
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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