A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112099



Internal ID21295365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62799676..62803120hg38UCSC Ensembl
Innerchr18:60466909..60470353hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383445
hg193445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv530n145
Supporting Variantsnssv14100953
Samplessample399
Known GenesPHLPP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112099
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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