A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458814



Internal ID21116367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89257044..89334866hg38UCSC Ensembl
chr11:88990212..89068034hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3877823
hg1977823
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188197
Samples
Known GenesNOX4, TYR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458814
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