A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111093



Internal ID21294359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190118019..190121259hg38UCSC Ensembl
Innerchr3:189835808..189839048hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg383241
hg193241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv838n145
Supporting Variantsnssv14107923, nssv14105984
Samplessample303, sample136
Known GenesLEPREL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111093
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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