A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112176



Internal ID21295442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68569726..68748292hg38UCSC Ensembl
Innerchr4:69435444..69614010hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38178567
hg19178567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv891n145
Supporting Variantsnssv14096648
Samplessample424
Known GenesUGT2B15
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112176
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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