A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513314



Internal ID15506050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45100632..45102438hg38UCSC Ensembl
Outerchr11:45122183..45123989hg19UCSC Ensembl
Outerchr11:45078759..45080565hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38781
hg19781
hg18781
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625701
Samples1
Known GenesPRDM11
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513314
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer