A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318360



Internal ID20851452
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 StatusM
Merged Variants
Supporting Variantsnssv18065726
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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