A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006287



Internal ID22067918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13809736..13829548hg38UCSC Ensembl
Outerchr9:13804581..13830117hg38UCSC Ensembl
Innerchr9:13809735..13829547hg19UCSC Ensembl
Outerchr9:13804580..13830116hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3825537
hg1925537
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154452
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006287
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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