A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110452



Internal ID21293718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8271524..8276216hg38UCSC Ensembl
Innerchr5:8271637..8276329hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg384693
hg194693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109168
Samplessample263
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110452
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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