A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063919



Internal ID18806450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10338676..10511951hg38UCSC Ensembl
Innerchr21:11000506..11173781hg19UCSC Ensembl
Innerchr21:10022377..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38173276
hg19173276
hg18173276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4369n100
Supporting Variantsnssv3585134, nssv3585135, nssv3585136
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063919
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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