A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065450



Internal ID19154669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18683769..18706106hg38UCSC Ensembl
Innerchr21:20056087..20078424hg19UCSC Ensembl
Innerchr21:18977958..19000295hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3822338
hg1922338
hg1822338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599691
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065450
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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