A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319603



Internal ID20852698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97796002..97822977hg38UCSC Ensembl
chr1:98261558..98288533hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3826976
hg1926976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202126
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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