A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv245n206



Internal ID22755549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31636911..31637015hg38UCSC Ensembl
chr19:32127817..32127921hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5529475, nsv5514964, nsv5519298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv245n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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