A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587494



Internal ID16028217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41369022..41390512hg38UCSC Ensembl
Innerchr21:42740949..42762439hg19UCSC Ensembl
Innerchr21:41662819..41684309hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3821491
hg1921491
hg1821491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7834n54
Supporting Variantsnssv946789
Samples
Known GenesMX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587494
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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