A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994614



Internal ID7079149
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586834
SamplesHuRef
Known GenesMYBL1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994614
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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