A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699342



Internal ID123008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77125192..77125211hg38UCSC Ensembl
chr14:77591535..77591554hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539094
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699342
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012644


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