A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889559



Internal ID167133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113906280..113906717hg38UCSC Ensembl
chr1:114448902..114449339hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430877
Supporting Variants
Samples
Known GenesDCLRE1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889559
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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