A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586350



Internal ID16373759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:57719257..57732490hg38UCSC Ensembl
Innerchr20:56294313..56307546hg19UCSC Ensembl
Innerchr20:55727719..55740952hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3813234
hg1913234
hg1813234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151379
SamplesHGDP00998
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586350
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