A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115150



Internal ID21298416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5249299..5254229hg38UCSC Ensembl
Innerchr11:5270529..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 Variantsdgv184n145
Supporting Variantsnssv14091167, nssv14091846
Samplessample78, sample206
Known GenesHBG1, HBG2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115150
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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