A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586834



Internal ID7058216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:66612585..66613058hg38UCSC Ensembl
Innerchr8:67524820..67525293hg19UCSC Ensembl
Innerchr8:67687374..67687847hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38474
hg19474
hg18474
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994614
Supporting Variants
SamplesHuRef
Known GenesMYBL1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586834
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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