A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv933n145



Internal ID22813949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153242134..153246547hg38UCSC Ensembl
chr4:154163286..154167699hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg384414
hg194414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112145, nsv3110338, nsv3111511, nsv3114756
Samplessample303, sample375, sample25, sample147, sample79, sample228
Known GenesTRIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv933n145
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer