A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586282



Internal ID16373691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54602439..54638276hg38UCSC Ensembl
Innerchr20:53218978..53254815hg19UCSC Ensembl
Innerchr20:52652385..52688222hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3835838
hg1935838
hg1835838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941573
Samples
Known GenesDOK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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