A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111960



Internal ID21295226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132918936..132921514hg38UCSC Ensembl
Innerchr11:132788831..132791409hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382579
hg192579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv234n145
Supporting Variantsnssv14093115
Samplessample313
Known GenesOPCML
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111960
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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