A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084846



Internal ID21994079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77416757..77416757hg38UCSC Ensembl
chr14:77883100..77883100hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604300
Samples
Known GenesNOXRED1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084846
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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