A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586978



Internal ID16027701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10324453..10520225hg38UCSC Ensembl
Innerchr21:10992232..11188004hg19UCSC Ensembl
Innerchr21:10014103..10209875hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38195773
hg19195773
hg18195773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944870
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586978
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer