A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279332



Internal ID20488550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65692333..65692386hg38UCSC Ensembl
chr14:66159051..66159104hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733013
Supporting Variants
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279332
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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