A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093165



Internal ID22002398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78871225..78871225hg38UCSC Ensembl
chr14:79337568..79337568hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617118
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093165
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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