A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687418



Internal ID111084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45540141..45540162hg38UCSC Ensembl
chr13:46114276..46114297hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550418
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687418
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.094072


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