A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105405



Internal ID21267777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102578214..102639430hg38UCSC Ensembl
Innerchr3:102297058..102358274hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3861217
hg1961217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113003
Supporting Variants
Samplessample116
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105405
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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