A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063253



Internal ID18805784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10404321..10601230hg38UCSC Ensembl
Innerchr21:10911227..11108136hg19UCSC Ensembl
Innerchr21:9933098..10130007hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38196910
hg19196910
hg18196910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4358n100
Supporting Variantsnssv3585030, nssv3585029
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063253
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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