A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587049



Internal ID6711745
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990743
Supporting Variants
SamplesHuRef
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA7
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587049
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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