A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586979



Internal ID16374388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10485790..10507714hg38UCSC Ensembl
Innerchr21:11004743..11026667hg19UCSC Ensembl
Innerchr21:10026614..10048538hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3821925
hg1921925
hg1821925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944871
Samples
Known GenesBAGE2, BAGE3, BAGE4, BAGE5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586979
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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