A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099837



Internal ID21287584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161515702..161612833hg38UCSC Ensembl
Innerchr1:161485492..161582623hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3897132
hg1997132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113160
Supporting Variants
Samplessample403
Known GenesFCGR2A, FCGR2C, FCGR3A, HSPA6, HSPA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099837
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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