A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091127



Internal ID21290547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124382699..124395800hg38UCSC Ensembl
Innerchr11:124252595..124265696hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3813102
hg1913102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113638
Supporting Variants
Samplessample60
Known GenesOR8B2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091127
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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