A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113864



Internal ID21297130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165630867..165635799hg38UCSC Ensembl
Innerchr1:165600104..165605036hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg384933
hg194933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085058, nssv14084757
Samplessample182, sample194
Known GenesMGST3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113864
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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