A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587082



Internal ID16374491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17334685..17372096hg38UCSC Ensembl
Innerchr21:18707004..18744415hg19UCSC Ensembl
Innerchr21:17628875..17666286hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3837412
hg1937412
hg1837412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv945517
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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