A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599690



Internal ID18897971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18683769..18705546hg38UCSC Ensembl
Innerchr21:20056087..20077864hg19UCSC Ensembl
Innerchr21:18977958..18999735hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3821778
hg1921778
hg1821778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058327
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)nssv3599690
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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