A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033294



Internal ID21942637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5409708..5471200hg38UCSC Ensembl
chr11:5430938..5492430hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861493
hg1961493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592082
Samples
Known GenesOR51B5, OR51I1, OR51I2, OR51Q1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033294
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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