A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626939



Internal ID15850471
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 StatusS
Merged Variantsnsv513687
Supporting Variants
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)nssv626939
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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