A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695964



Internal ID119630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60447122..60474491hg38UCSC Ensembl
chr14:60913840..60941209hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3827370
hg1927370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562885
Supporting Variants
Samples
Known GenesC14orf39
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695964
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.445659


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