A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586300



Internal ID6710996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161513165..161676614hg38UCSC Ensembl
Innerchr1:161482955..161646404hg19UCSC Ensembl
Innerchr1:159749579..159913028hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38163450
hg19163450
hg18163450
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997087
Supporting Variants
SamplesHuRef
Known GenesFCGR2A, FCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA6, HSPA7
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586300
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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