A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110699



Internal ID21293965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68303713..68617463hg38UCSC Ensembl
Innerchr4:69169431..69483181hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38313751
hg19313751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv885n145
Supporting Variantsnssv14107274
Samplessample31
Known GenesTMPRSS11E, UGT2B17, YTHDC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110699
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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