A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510190



Internal ID286817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79188525..79199381hg38UCSC Ensembl
chr14:79654868..79665724hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3810857
hg1910857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699458
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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