A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111147



Internal ID21294413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:46570842..46580346hg38UCSC Ensembl
Innerchr11:46592392..46601896hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389505
hg199505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093145
Samplessample322
Known GenesAMBRA1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111147
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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