A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994079



Internal ID6730034
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4e180
Supporting Variantsessv3586877
SamplesHuRef
Known GenesBCAR3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994079
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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