A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794354



Internal ID21239692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55331798..55331798hg38UCSC Ensembl
chr14:55798516..55798516hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691596
Samples
Known GenesFBXO34
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794354
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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