A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058893



Internal ID18801424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10388379..10509926hg38UCSC Ensembl
Innerchr21:11002531..11124078hg19UCSC Ensembl
Innerchr21:10024402..10145949hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38121548
hg19121548
hg18121548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4370n100
Supporting Variantsnssv3585157
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)nsv1058893
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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