A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112900



Internal ID21296166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114639414..114684125hg38UCSC Ensembl
Innerchr5:113975111..114019822hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3844712
hg1944712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097316
Samplessample87
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112900
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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