A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17018130



Internal ID79733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135946936..135947177hg38UCSC Ensembl
chr8:136959179..136959420hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17018130
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.019201


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