A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154481



Internal ID22084986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37504706..37514035hg38UCSC Ensembl
Outerchr9:37502112..37515714hg38UCSC Ensembl
Innerchr9:37504703..37514032hg19UCSC Ensembl
Outerchr9:37502109..37515711hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3813603
hg1913603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005294, nssv4005293
Samples
Known GenesFBXO10, POLR1E
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154481
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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