A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586135



Internal ID16373544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46126472..46168923hg38UCSC Ensembl
Innerchr20:44755111..44797562hg19UCSC Ensembl
Innerchr20:44188518..44230969hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3842452
hg1942452
hg1842452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940872
Samples
Known GenesCD40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586135
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