A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698136



Internal ID121802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63545828..63566395hg38UCSC Ensembl
chr14:64012546..64033113hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3820568
hg1920568
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698136
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.105838


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer