A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586882



Internal ID16374291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10648253..10813996hg38UCSC Ensembl
Innerchr21:10698461..10864204hg19UCSC Ensembl
Innerchr21:9720332..9886075hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38165744
hg19165744
hg18165744
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7727n54
Supporting Variantsnssv944767
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586882
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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