A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116005



Internal ID21299271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151770241..151773726hg38UCSC Ensembl
Innerchr5:151149802..151153287hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383486
hg193486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109044
Samplessample224
Known GenesG3BP1, LOC100652758
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116005
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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