A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116082



Internal ID21299348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:46117789..46123874hg38UCSC Ensembl
Innerchr11:46139340..46145425hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg386086
hg196086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091037
Samplessample138
Known GenesPHF21A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116082
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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