A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721815



Internal ID145481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15874303..15906589hg38UCSC Ensembl
chr19:15985113..16017399hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3832287
hg1932287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529925
Supporting Variants
Samples
Known GenesCYP4F2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721815
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