A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv562n145



Internal ID22813578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30220853..30230771hg38UCSC Ensembl
chr19:30711760..30721678hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg389919
hg199919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111582, nsv3116199, nsv3111212, nsv3111318
Samplessample346, sample63, sample412, sample360
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv562n145
Frequency
Sample Size467
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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