A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4012196



Internal ID22073827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98259011..98283337hg38UCSC Ensembl
Outerchr15:98258508..98289411hg38UCSC Ensembl
Innerchr15:98802240..98826566hg19UCSC Ensembl
Outerchr15:98801737..98832640hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3830904
hg1930904
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155216
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4012196
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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