A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17470344



Internal ID22528234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89453310..89459846hg38UCSC Ensembl
chr14:89919654..89926190hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg386537
hg196537
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851703
Supporting Variants
Samples
Known GenesFOXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17470344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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