A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586879



Internal ID16374288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10652006..10813996hg38UCSC Ensembl
Innerchr21:10698461..10860451hg19UCSC Ensembl
Innerchr21:9720332..9882322hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38161991
hg19161991
hg18161991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7727n54
Supporting Variantsnssv944759, nssv944761, nssv944760
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586879
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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