A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599691



Internal ID18897972
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 StatusS
Merged Variantsnsv1065450
Supporting Variants
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)nssv3599691
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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