A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020616



Internal ID22082247
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156299
Supporting Variants
Samples
Known GenesTERT
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020616
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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