A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587459



Internal ID16374868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35735148..35827236hg38UCSC Ensembl
Innerchr21:37107446..37199534hg19UCSC Ensembl
Innerchr21:36029316..36121404hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3892089
hg1992089
hg1892089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151615
SamplesHGDP01353
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587459
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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