A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469736



Internal ID22527626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89616456..89618106hg38UCSC Ensembl
chr14:90082800..90084450hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381651
hg191651
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853511
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469736
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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