A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513335



Internal ID15852757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118807378..118807747hg38UCSC Ensembl
Outerchr11:118678087..118678456hg19UCSC Ensembl
Outerchr11:118183297..118183666hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381175
hg191175
hg181175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625726
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)nsv513335
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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