A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693363



Internal ID117029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80364961..80364961hg38UCSC Ensembl
chr13:80939096..80939096hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693363
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.006418


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