A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513341



Internal ID15506077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:126276166..126276319hg38UCSC Ensembl
Outerchr11:126146061..126146214hg19UCSC Ensembl
Outerchr11:125651271..125651424hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381772
hg191772
hg181772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625732
Samples1
Known GenesFOXRED1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513341
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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