A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17719458



Internal ID143124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73894786..73894925hg38UCSC Ensembl
chr18:71562021..71562160hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17719458
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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