A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107722



Internal ID21284326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:79511302..79515709hg38UCSC Ensembl
Innerchr5:78807125..78811532hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg384408
hg194408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117932
Supporting Variants
Samplessample360
Known GenesHOMER1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107722
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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