A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563776



Internal ID7034876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:21034679..21052786hg38UCSC Ensembl
Outerchr8:20892190..20910297hg19UCSC Ensembl
Outerchr8:20936470..20954577hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3818108
hg1918108
hg1818108
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995988
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563776
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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