A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111494



Internal ID21294760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:154384733..154446563hg38UCSC Ensembl
Innerchr1:154357209..154419039hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3861831
hg1961831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104874
Samplessample52
Known GenesIL6R
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111494
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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