A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111419



Internal ID21294685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177179262..177184265hg38UCSC Ensembl
Innerchr3:176897050..176902053hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385004
hg195004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106529
Samplessample161
Known GenesTBL1XR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111419
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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