A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067014



Internal ID19156233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18683769..18711118hg38UCSC Ensembl
Innerchr21:20056087..20083436hg19UCSC Ensembl
Innerchr21:18977958..19005307hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3827350
hg1927350
hg1827350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599726
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)nsv1067014
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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