A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3349780



Internal ID15196762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1894254..1939849hg38UCSC Ensembl
Innerchr11:1896244..1938269hg38UCSC Ensembl
Outerchr11:1894144..1939969hg38UCSC Ensembl
chr11:1915484..1961079hg19UCSC Ensembl
Innerchr11:1917474..1959499hg19UCSC Ensembl
Outerchr11:1915374..1961199hg19UCSC Ensembl
chr11:1872060..1917655hg18UCSC Ensembl
Innerchr11:1874050..1916075hg18UCSC Ensembl
Outerchr11:1871950..1917775hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3845596
hg1945596
hg1845596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808557
SamplesNA12878
Known GenesTNNT3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3349780
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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