A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107723



Internal ID21284327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98770910..98776517hg38UCSC Ensembl
Innerchr5:98106614..98112221hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg385608
hg195608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115519
Supporting Variants
Samplessample360
Known GenesRGMB, RGMB-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107723
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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