A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111511



Internal ID21294777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153242134..153245402hg38UCSC Ensembl
Innerchr4:154163286..154166554hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383269
hg193269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv933n145
Supporting Variantsnssv14107567, nssv14090451, nssv14093512
Samplessample303, sample147, sample79
Known GenesTRIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111511
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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