A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587457



Internal ID16374866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35481219..35523898hg38UCSC Ensembl
Innerchr21:36853517..36896196hg19UCSC Ensembl
Innerchr21:35775387..35818066hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3842680
hg1942680
hg1842680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946757
Samples
Known GenesLOC100506403
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587457
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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