A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116103



Internal ID21299369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3926334..3949759hg38UCSC Ensembl
Innerchr11:3947564..3970989hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3823426
hg1923426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv180n145
Supporting Variantsnssv14091832
Samplessample198
Known GenesSTIM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116103
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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