A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586209



Internal ID16026932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53587523..53672704hg38UCSC Ensembl
Innerchr20:52204062..52289243hg19UCSC Ensembl
Innerchr20:51637469..51722650hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3885182
hg1985182
hg1885182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941151
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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