A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv184n145



Internal ID22813200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5249299..5254229hg38UCSC Ensembl
chr11:5270529..5275459hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384931
hg194931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115150, nsv3117251
Samplessample379, sample78, sample206, sample5
Known GenesHBG1, HBG2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv184n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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