A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065659



Internal ID20632699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97215450..97227371hg38UCSC Ensembl
chr1:97681006..97692927hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3811922
hg1911922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315851
Supporting Variants
Samples
Known GenesDPYD, DPYD-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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