A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105547



Internal ID21288170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179145687..179152384hg38UCSC Ensembl
Innerchr3:178863475..178870172hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg386698
hg196698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114578
Supporting Variants
Samplessample412
Known GenesPIK3CA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105547
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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