A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796404



Internal ID21241742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87332618..87332618hg38UCSC Ensembl
chr16:87366224..87366224hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682081
Samples
Known GenesFBXO31
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796404
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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