A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587363



Internal ID16374772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31368793..31390097hg38UCSC Ensembl
Innerchr21:32741108..32762410hg19UCSC Ensembl
Innerchr21:31662979..31684281hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3821305
hg1921303
hg1821303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946605
Samples
Known GenesTIAM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587363
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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