A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586886



Internal ID16027609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10465168..10813996hg38UCSC Ensembl
Innerchr21:10698461..11047289hg19UCSC Ensembl
Innerchr21:9720332..10069160hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38348829
hg19348829
hg18348829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7728n54
Supporting Variantsnssv944774, nssv944773
Samples
Known GenesBAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586886
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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