A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082633



Internal ID21286321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:154032543..154151691hg38UCSC Ensembl
Innerchr5:153412103..153531251hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38119149
hg19119149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116373
Supporting Variants
Samplessample386
Known GenesFAM114A2, MFAP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082633
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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