A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154332



Internal ID22084837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:26643835..26667459hg38UCSC Ensembl
Outerchr8:26641135..26674412hg38UCSC Ensembl
Innerchr8:26501351..26524976hg19UCSC Ensembl
Outerchr8:26498651..26531929hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3833278
hg1933279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv284n97
Supporting Variantsnssv4004263
Samples
Known GenesDPYSL2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154332
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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