A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097599



Internal ID21285042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161532773..161673745hg38UCSC Ensembl
Innerchr1:161502563..161643535hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38140973
hg19140973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117262
Supporting Variants
Samplessample369
Known GenesFCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097599
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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