A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586583



Internal ID16373992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63595728..63609618hg38UCSC Ensembl
Innerchr20:62227081..62240971hg19UCSC Ensembl
Innerchr20:61697525..61711415hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3813891
hg1913891
hg1813891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7670n54
Supporting Variantsnssv943762
Samples
Known GenesGMEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586583
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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