A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586090



Internal ID16373499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45575651..45583998hg38UCSC Ensembl
Innerchr20:44204290..44212637hg19UCSC Ensembl
Innerchr20:43637704..43646051hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg388348
hg198348
hg188348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7589n54
Supporting Variantsnssv940772, nssv940771
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586090
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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