A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114114



Internal ID21297380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:44732337..44738728hg38UCSC Ensembl
Innerchr20:43360978..43367369hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386392
hg196392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099866
Samplessample158
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114114
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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