A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513418



Internal ID15852840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:97787183..97788777hg38UCSC Ensembl
Outerchr14:98253520..98255114hg19UCSC Ensembl
Outerchr14:97323273..97324867hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38891
hg19891
hg18891
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625816
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)nsv513418
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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