A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156299



Internal ID22084775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1274224..1288579hg38UCSC Ensembl
Outerchr5:1269250..1299214hg38UCSC Ensembl
Innerchr5:1274339..1288694hg19UCSC Ensembl
Outerchr5:1269365..1299329hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3829965
hg1929965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020616
Samples
Known GenesTERT
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156299
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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