A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110927



Internal ID21294193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26855168..26862734hg38UCSC Ensembl
Innerchr4:26856790..26864356hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg387567
hg197567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869n145
Supporting Variantsnssv14094703
Samplessample360
Known GenesSTIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110927
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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