A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861105



Internal ID22636040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6758091..6802054hg38UCSC Ensembl
chr11:6779322..6823285hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3843964
hg1943964
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459203
Samples
Known GenesOR2AG1, OR2AG2, OR6A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861105
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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