A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv370n172



Internal ID22814744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31192095..31211094hg38UCSC Ensembl
chr19:31683001..31702000hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3819000
hg1919000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4432810, nsv4432811
SamplesMDQ045, BTQ038, BTQ055, MDQ010, BTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv370n172
Frequency
Sample Size15
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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