A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156300



Internal ID22084776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1274224..1351423hg38UCSC Ensembl
Outerchr5:1269250..1359823hg38UCSC Ensembl
Innerchr5:1274339..1351538hg19UCSC Ensembl
Outerchr5:1269365..1359938hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3890574
hg1990574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020617
Samples
Known GenesCLPTM1L, MIR4457, TERT
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156300
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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