A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113412



Internal ID21296678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124383843..124395800hg38UCSC Ensembl
Innerchr11:124253739..124265696hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3811958
hg1911958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv229n145
Supporting Variantsnssv14093194, nssv14093027
Samplessample345, sample278
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113412
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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