A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015303



Internal ID77856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117856222..117864222hg38UCSC Ensembl
chr8:118868461..118876461hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482654
Supporting Variants
Samples
Known GenesEXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015303
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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