A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697670



Internal ID121336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89024358..89068675hg38UCSC Ensembl
chr14:89490702..89535019hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3844318
hg1944318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697670
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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