A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513313



Internal ID15852735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:44663369..44665204hg38UCSC Ensembl
Outerchr11:44684919..44686754hg19UCSC Ensembl
Outerchr11:44641495..44643330hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381022
hg191022
hg181022
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625700
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)nsv513313
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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