A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489145



Internal ID21146698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78748169..78780458hg38UCSC Ensembl
chr14:79214512..79246801hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3832290
hg1932290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195739
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer