A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105929



Internal ID21291879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:42259633..42364745hg38UCSC Ensembl
Innerchr1:42725304..42830416hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38105113
hg19105113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116348
Supporting Variants
Samplessample80
Known GenesFOXJ3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105929
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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