A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv862n145



Internal ID22813878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18119397..18125441hg38UCSC Ensembl
chr4:18121020..18127064hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386045
hg196045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110546, nsv3114876
Samplessample241, sample266, sample171, sample44
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv862n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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