A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513321



Internal ID15852743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:66598298..66598615hg38UCSC Ensembl
Outerchr11:66365769..66366086hg19UCSC Ensembl
Outerchr11:66122345..66122662hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38943
hg19943
hg18943
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625708
Samples1
Known GenesCCS
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513321
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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