A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065726



Internal ID20632766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97698917..97699180hg38UCSC Ensembl
chr1:98164473..98164736hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318360
Supporting Variants
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00035


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