A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587369



Internal ID16374778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33244240..33245738hg38UCSC Ensembl
Innerchr21:34616545..34618043hg19UCSC Ensembl
Innerchr21:33538415..33539913hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946610
Samples
Known GenesIFNAR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587369
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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