A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv869n145



Internal ID22813885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26855168..26863656hg38UCSC Ensembl
chr4:26856790..26865278hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388489
hg198489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110927, nsv3116870
Samplessample412, sample360
Known GenesSTIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv869n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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