A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112816



Internal ID21296082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:188574..198707hg38UCSC Ensembl
Innerchr5:188689..198822hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3810134
hg1910134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107730
Samplessample362
Known GenesLRRC14B, PLEKHG4B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112816
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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