A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586885



Internal ID16027608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10511675..10813996hg38UCSC Ensembl
Innerchr21:10698461..11000782hg19UCSC Ensembl
Innerchr21:9720332..10022653hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38302322
hg19302322
hg18302322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7728n54
Supporting Variantsnssv944772
Samples
Known GenesTPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586885
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