A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17018696



Internal ID80104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133024791..133024842hg38UCSC Ensembl
chr8:134037036..134037087hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142903
Supporting Variants
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17018696
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002659


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