A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494866



Internal ID271996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79841755..79877569hg38UCSC Ensembl
chr14:80308098..80343912hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3835815
hg1935815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698954
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494866
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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