A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065702



Internal ID20632742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97552042..97595395hg38UCSC Ensembl
chr1:98017598..98060951hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3843354
hg1943354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331662
Supporting Variants
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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