A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586877



Internal ID6711573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93822771..93825611hg38UCSC Ensembl
Innerchr1:94288327..94291167hg19UCSC Ensembl
Innerchr1:94060915..94063755hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382841
hg192841
hg182841
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994079
Supporting Variants
SamplesHuRef
Known GenesBCAR3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586877
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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