A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991674



Internal ID6727638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:62821895..62838624hg38UCSC Ensembl
Outerchr11:62589367..62606096hg19UCSC Ensembl
Outerchr11:62345943..62362672hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3816730
hg1916730
hg1816730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565578
SamplesHuRef
Known GenesSTX5, WDR74
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991674
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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