A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587360



Internal ID16374769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30953268..31006158hg38UCSC Ensembl
Innerchr21:32325587..32378477hg19UCSC Ensembl
Innerchr21:31247458..31300348hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3852891
hg1952891
hg1852891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946602
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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