A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv321n145



Internal ID22813337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25484540..25489766hg38UCSC Ensembl
chr14:25953746..25958972hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385227
hg195227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112161, nsv3116643
Samplessample69, sample146, sample256, sample96, sample45, sample107
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv321n145
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