A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv886n145



Internal ID22813902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68475301..68552993hg38UCSC Ensembl
chr4:69341019..69418711hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3877693
hg1977693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111731, nsv3112439
Samplessample91, sample34
Known GenesTMPRSS11E, UGT2B17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv886n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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