A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005293



Internal ID22066924
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154481
Supporting Variants
Samples
Known GenesFBXO10, POLR1E
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005293
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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