A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586084



Internal ID16373493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45575651..45577280hg38UCSC Ensembl
Innerchr20:44204290..44205919hg19UCSC Ensembl
Innerchr20:43637704..43639333hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381630
hg191630
hg181630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7587n54
Supporting Variantsnssv940722, nssv940723
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586084
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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