A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015290



Internal ID77851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117697110..117697110hg38UCSC Ensembl
chr8:118709349..118709349hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394236
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015290
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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