A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094687



Internal ID21405941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55329134..55329134hg38UCSC Ensembl
chr14:55795852..55795852hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646053
Supporting Variants
SamplesHG00512
Known GenesFBXO34
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094687
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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