A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587157



Internal ID16374566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18755513..18778825hg38UCSC Ensembl
Innerchr21:20127831..20151143hg19UCSC Ensembl
Innerchr21:19049702..19073014hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3823313
hg1923313
hg1823313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150987
SamplesHGDP00920
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587157
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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