A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990743



Internal ID7076874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161550050..161649676hg38UCSC Ensembl
Innerchr1:161519840..161619466hg19UCSC Ensembl
Innerchr1:159786464..159886090hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3899627
hg1999627
hg1899627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587049
SamplesHuRef
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA7
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990743
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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