A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587640



Internal ID16028363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42513540..42514398hg38UCSC Ensembl
Innerchr21:43933650..43934508hg19UCSC Ensembl
Innerchr21:42806719..42807577hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38859
hg19859
hg18859
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7863n54
Supporting Variantsnssv947367, nssv947369, nssv947368
Samples
Known GenesSLC37A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587640
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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