A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv536n172



Internal ID22814910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167126818..167131494hg38UCSC Ensembl
chr3:166844606..166849282hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg384677
hg194677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4433938, nsv4433940, nsv4433939
SamplesBTQ038, BTQ055, BTQ016, NB07, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv536n172
Frequency
Sample Size15
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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