A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000906



Internal ID7066035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:69960754..69976928hg38UCSC Ensembl
Outerchr8:70872989..70889163hg19UCSC Ensembl
Outerchr8:71035543..71051717hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3816175
hg1916175
hg1816175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564661
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000906
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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