A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586890



Internal ID16374299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10651108..10809201hg38UCSC Ensembl
Innerchr21:10703256..10861349hg19UCSC Ensembl
Innerchr21:9725127..9883220hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38158094
hg19158094
hg18158094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7727n54
Supporting Variantsnssv944779
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586890
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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