A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084757



Internal ID21272774
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 StatusS
Merged Variantsnsv3113864
Supporting Variants
Samplessample182
Known GenesMGST3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084757
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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