A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938911



Internal ID16232867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21926142..21971209hg38UCSC Ensembl
Innerchr20:21906780..21951847hg19UCSC Ensembl
Innerchr20:21854780..21899847hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3845068
hg1945068
hg1845068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585715
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938911
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