A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925089



Internal ID22700316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6758182..6872395hg38UCSC Ensembl
chr11:6779413..6893626hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38114214
hg19114214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352871
Samples
Known GenesOR10A2, OR10A5, OR2AG1, OR2AG2, OR6A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925089
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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