A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587842



Internal ID16028565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45221102..45250837hg38UCSC Ensembl
Innerchr21:46641017..46670752hg19UCSC Ensembl
Innerchr21:45465445..45495180hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3829736
hg1929736
hg1829736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948531
Samples
Known GenesADARB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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