A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908450



Internal ID6422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97419208..97422073hg38UCSC Ensembl
chr1:97884764..97887629hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382866
hg192866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431737
Supporting Variants
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908450
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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