A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509197



Internal ID285860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65537636..65538811hg38UCSC Ensembl
chr14:66004354..66005529hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381176
hg191176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697726
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509197
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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