A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586650



Internal ID16374059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63830660..63835962hg38UCSC Ensembl
Innerchr20:62462013..62467315hg19UCSC Ensembl
Innerchr20:61932457..61937759hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385303
hg195303
hg185303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7687n54
Supporting Variantsnssv943892, nssv943891
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586650
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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