A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093054



Internal ID22002287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76518525..76518525hg38UCSC Ensembl
chr14:76984868..76984868hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093054
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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