A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058240



Internal ID18800771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10348542..10473197hg38UCSC Ensembl
Innerchr21:11039260..11163915hg19UCSC Ensembl
Innerchr21:10061131..10185786hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38124656
hg19124656
hg18124656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4372n100
Supporting Variantsnssv3585163
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)nsv1058240
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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