A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099981



Internal ID21287648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161546322..161649467hg38UCSC Ensembl
Innerchr1:161516112..161619257hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38103146
hg19103146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114025
Supporting Variants
Samplessample404
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099981
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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