A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059291



Internal ID18801822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10348542..10775598hg38UCSC Ensembl
Innerchr21:10736859..11163915hg19UCSC Ensembl
Innerchr21:9758730..10185786hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38427057
hg19427057
hg18427057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3583785
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)nsv1059291
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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