A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015179



Internal ID77774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109085101..109085101hg38UCSC Ensembl
chr8:110097330..110097330hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015179
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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