A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113992



Internal ID21297258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22094699..22116676hg38UCSC Ensembl
Innerchr18:19674660..19696637hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3821978
hg1921978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100110
Samplessample253
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113992
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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