A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154967



Internal ID22085472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98232964..98243833hg38UCSC Ensembl
Outerchr13:98230682..98248924hg38UCSC Ensembl
Innerchr13:98885218..98896087hg19UCSC Ensembl
Outerchr13:98882936..98901178hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3818243
hg1918243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008299
Samples
Known GenesFARP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154967
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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