A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722589



Internal ID146255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28443502..28449862hg38UCSC Ensembl
chr19:28934409..28940769hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg386361
hg196361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722589
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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