A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694914



Internal ID118580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57686141..57691476hg38UCSC Ensembl
chr14:58152859..58158194hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg385336
hg195336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507758
Supporting Variants
Samples
Known GenesSLC35F4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694914
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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