A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115991



Internal ID21299257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161532773..161672531hg38UCSC Ensembl
Innerchr1:161502563..161642321hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38139759
hg19139759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv81n145
Supporting Variantsnssv14085169
Samplessample196
Known GenesFCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115991
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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