A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587391



Internal ID16028114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33322014..33324562hg38UCSC Ensembl
Innerchr21:34694319..34696867hg19UCSC Ensembl
Innerchr21:33616189..33618737hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382549
hg192549
hg182549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7818n54
Supporting Variantsnssv946639
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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