A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114756



Internal ID21298022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153242134..153246000hg38UCSC Ensembl
Innerchr4:154163286..154167152hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383867
hg193867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv933n145
Supporting Variantsnssv14094813
Samplessample375
Known GenesTRIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114756
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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