A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592082



Internal ID21784125
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 StatusS
Merged Variantsnsv6033294
Supporting Variants
Samples
Known GenesOR51B5, OR51I1, OR51I2, OR51Q1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592082
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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