A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064392



Internal ID19153611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18682927..18711118hg38UCSC Ensembl
Innerchr21:20055245..20083436hg19UCSC Ensembl
Innerchr21:18977116..19005307hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3828192
hg1928192
hg1828192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599687
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)nsv1064392
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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