A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626941



Internal ID15850473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1894063..1939908hg38UCSC Ensembl
Outerchr11:1915293..1961138hg19UCSC Ensembl
Outerchr11:1871869..1917714hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3845846
hg1945846
hg1845846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513689
Supporting Variants
Samples1
Known GenesTNNT3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626941
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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