A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090130



Internal ID21477747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55331803..55331803hg38UCSC Ensembl
chr14:55798521..55798521hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663618
Supporting Variants
SamplesHG03486
Known GenesFBXO34
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090130
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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