A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084291



Internal ID21993524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79462861..79462861hg38UCSC Ensembl
chr14:79929204..79929204hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613931
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084291
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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