A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586659



Internal ID16374068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63831097..63836435hg38UCSC Ensembl
Innerchr20:62462450..62467788hg19UCSC Ensembl
Innerchr20:61932894..61938232hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385339
hg195339
hg185339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7687n54
Supporting Variantsnssv943909, nssv943908, nssv943907
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586659
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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