A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv229n145



Internal ID22813245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124382699..124395800hg38UCSC Ensembl
chr11:124252595..124265696hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3813102
hg1913102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113412, nsv3113638
Samplessample60, sample345, sample278
Known GenesOR8B2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv229n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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