A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117864



Internal ID21301130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68475309..68615601hg38UCSC Ensembl
Innerchr4:69341027..69481319hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38140293
hg19140293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv887n145
Supporting Variantsnssv14093335
Samplessample271
Known GenesTMPRSS11E, UGT2B17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117864
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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