A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110376



Internal ID21293642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115370534..115386867hg38UCSC Ensembl
Innerchr5:114706231..114722564hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3816334
hg1916334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv984n145
Supporting Variantsnssv14109371
Samplessample324
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110376
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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