A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002169



Internal ID6714303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:125429555..125430364hg38UCSC Ensembl
Innerchr8:126441797..126442606hg19UCSC Ensembl
Innerchr8:126510979..126511788hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38810
hg19810
hg18810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587201
SamplesHuRef
Known GenesTRIB1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002169
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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