A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065722



Internal ID20632762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97688301..97689400hg38UCSC Ensembl
chr1:98153857..98154956hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321838
Supporting Variants
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer