A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698769



Internal ID122435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98124260..98142544hg38UCSC Ensembl
chr14:98590597..98608881hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3818285
hg1918285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698769
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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