A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110269



Internal ID21293535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26858774..26862728hg38UCSC Ensembl
Innerchr4:26860396..26864350hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383955
hg193955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv870n145
Supporting Variantsnssv14090403
Samplessample139
Known GenesSTIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110269
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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