A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517045



Internal ID293478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17821981..17822928hg38UCSC Ensembl
chr19:17932790..17933737hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517045
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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