A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429466



Internal ID208314
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 StatusM
Merged Variants
Supporting Variantsnssv16908485
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429466
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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