A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077262



Internal ID21401785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117150960..117150960hg38UCSC Ensembl
chr12:117588765..117588765hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661757
Supporting Variants
SamplesHG00096
Known GenesFBXO21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077262
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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