A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005290



Internal ID22066921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32082228..32088859hg38UCSC Ensembl
Outerchr9:32079198..32090240hg38UCSC Ensembl
Innerchr9:32082226..32088857hg19UCSC Ensembl
Outerchr9:32079196..32090238hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3811043
hg1911043
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154478
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005290
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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