A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908485



Internal ID6446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97734784..97748631hg38UCSC Ensembl
chr1:98200340..98214187hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3813848
hg1913848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429466
Supporting Variants
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908485
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