A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586222



Internal ID16026945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53857140..53889841hg38UCSC Ensembl
Innerchr20:52473679..52506380hg19UCSC Ensembl
Innerchr20:51907086..51939787hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3832702
hg1932702
hg1832702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941219
Samples
Known GenesSUMO1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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