A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008299



Internal ID22069930
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 Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154967
Supporting Variants
Samples
Known GenesFARP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008299
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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