A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513687



Internal ID15853108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:310047..317793hg38UCSC Ensembl
Outerchr11:310047..317793hg19UCSC Ensembl
Outerchr11:300047..307793hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387747
hg197747
hg187747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626939
Samples1
Known GenesIFITM1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513687
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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