A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585715



Internal ID16373124
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 StatusM
Merged Variantsdgv7518n54
Supporting Variantsnssv938911
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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