A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110622



Internal ID21293888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68871407..68873564hg38UCSC Ensembl
Innerchr11:68638875..68641032hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg382158
hg192158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093092, nssv14093249, nssv14090225
Samplessample369, sample387, sample304
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110622
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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