A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105026



Internal ID21288674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161515702..161673745hg38UCSC Ensembl
Innerchr1:161485492..161643535hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38158044
hg19158044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111292
Supporting Variants
Samplessample42
Known GenesFCGR2A, FCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA6, HSPA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105026
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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