A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108522



Internal ID21283852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112894078..112915950hg38UCSC Ensembl
Innerchr3:112612925..112634797hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3821873
hg1921873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111019
Supporting Variants
Samplessample350
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108522
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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