A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586193



Internal ID16026916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52060890..52082766hg38UCSC Ensembl
Innerchr20:50677429..50699305hg19UCSC Ensembl
Innerchr20:50110836..50132712hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3821877
hg1921877
hg1821877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150960
SamplesHGDP00925
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586193
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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