A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854362



Internal ID22629297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55293614..55295913hg38UCSC Ensembl
chr14:55760332..55762631hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465895
Samples
Known GenesFBXO34
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854362
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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