A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796350



Internal ID21241688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89566207..89566207hg38UCSC Ensembl
chr16:89632615..89632615hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689895
Samples
Known GenesRPL13
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796350
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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