A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088160



Internal ID21491367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87384733..87384733hg38UCSC Ensembl
chr16:87418339..87418339hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658127
Supporting Variants
SamplesNA19238
Known GenesFBXO31
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088160
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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