A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114502



Internal ID21297768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97532962..97601658hg38UCSC Ensembl
Innerchr11:97403962..97472658hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3868697
hg1968697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091038
Samplessample138
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114502
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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