A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116466



Internal ID21299732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:69110669..69349884hg38UCSC Ensembl
Innerchr4:69976387..70215602hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38239216
hg19239216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093543
Samplessample310
Known GenesUGT2B11, UGT2B28, UGT2B7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116466
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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