A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114025



Internal ID21297291
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 StatusM
Merged Variantsdgv81n145
Supporting Variantsnssv14102383, nssv14098090, nssv14099981
Samplessample365, sample404, sample43
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114025
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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