A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586653



Internal ID16374062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63830660..63836381hg38UCSC Ensembl
Innerchr20:62462013..62467734hg19UCSC Ensembl
Innerchr20:61932457..61938178hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385722
hg195722
hg185722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7687n54
Supporting Variantsnssv943895, nssv943896
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586653
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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