A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3297828



Internal ID11317494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42332482..42336482hg38UCSC Ensembl
Innerchr8:42190000..42194000hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv36e209
Supporting Variantsessv7567395
SamplesHuRef
Known GenesIKBKB
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3297828
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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