A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586893



Internal ID16374302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10594687..10804226hg38UCSC Ensembl
Innerchr21:10708231..10917770hg19UCSC Ensembl
Innerchr21:9730102..9939641hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38209540
hg19209540
hg18209540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7731n54
Supporting Variantsnssv944782
Samples
Known GenesTPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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