A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097267



Internal ID21291695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:21574637..21600217hg38UCSC Ensembl
Innerchr5:21574746..21600326hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3825581
hg1925581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111716
Supporting Variants
Samplessample78
Known GenesGUSBP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097267
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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