A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011096



Internal ID6723186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1890698..1939961hg38UCSC Ensembl
Outerchr11:1911928..1961191hg19UCSC Ensembl
Outerchr11:1868504..1917767hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3849264
hg1949264
hg1849264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565289
SamplesHuRef
Known GenesLSP1, TNNT3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011096
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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