A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17719850



Internal ID143516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78947003..78947173hg38UCSC Ensembl
chr18:76707003..76707173hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17719850
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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