A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010584



Internal ID6722674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68506420..68568955hg38UCSC Ensembl
Innerchr4:69372138..69434673hg19UCSC Ensembl
Innerchr4:69054733..69117268hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3862536
hg1962536
hg1862536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586154
SamplesHuRef
Known GenesUGT2B17
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010584
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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