A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113158



Internal ID21296424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58225879..58230761hg38UCSC Ensembl
Innerchr20:56800935..56805817hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg384883
hg194883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099932
Samplessample208
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113158
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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