A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946156



Internal ID16240112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18688618..18702806hg38UCSC Ensembl
Innerchr21:20060936..20075124hg19UCSC Ensembl
Innerchr21:18982807..18996995hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3814189
hg1914189
hg1814189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587154
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946156
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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