A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510615



Internal ID287226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124382364..124396364hg38UCSC Ensembl
chr11:124252260..124266260hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3814001
hg1914001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053692
Samples
Known GenesOR8B2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510615
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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