A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513694



Internal ID15506429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:66248891..66252272hg38UCSC Ensembl
Outerchr11:66016362..66019743hg19UCSC Ensembl
Outerchr11:65772938..65776319hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383382
hg193382
hg183382
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626946
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513694
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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