A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585242



Internal ID16372651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580578..1613627hg38UCSC Ensembl
Innerchr20:1561224..1594273hg19UCSC Ensembl
Innerchr20:1509224..1542273hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3833050
hg1933050
hg1833050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7433n54
Supporting Variantsnssv936088, nssv936120, nssv936126, nssv936113, nssv936116, nssv936091, nssv936121, nssv936080, nssv936118, nssv936124, nssv936105, nssv936093, nssv936101, nssv936104, nssv936127, nssv936112, nssv936125, nssv936110, nssv936117, nssv936123, nssv936111, nssv936083, nssv936085, nssv936103, nssv936098, nssv936115, nssv936109, nssv936079, nssv936084, nssv936087, nssv936097, nssv936086, nssv936108, nssv936119, nssv936114, nssv936089, nssv936096, nssv936094, nssv936090, nssv936107, nssv936095, nssv936092, nssv936106, nssv936100, nssv936099, nssv936102, nssv936082, nssv936122, nssv936081
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585242
Frequency
Sample Size17421
Observed Gain49
Observed Loss0
Observed Complex0
Frequencyn/a


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