A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111233



Internal ID21294499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231330121..231383966hg38UCSC Ensembl
Innerchr2:232194833..232248677hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3853846
hg1953845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105639
Samplessample198
Known GenesARMC9, MIR4777
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111233
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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