A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315691



Internal ID20848763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97687391..97688391hg38UCSC Ensembl
chr1:98152947..98153947hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202125
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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