A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723357



Internal ID147023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39806778..39807648hg38UCSC Ensembl
chr19:40297418..40298288hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520345
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723357
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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