A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469737



Internal ID22527627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89616581..89617906hg38UCSC Ensembl
chr14:90082925..90084250hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381326
hg191326
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847825
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469737
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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