A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006118



Internal ID22067749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6089978..6121460hg38UCSC Ensembl
Outerchr9:6089129..6124250hg38UCSC Ensembl
Innerchr9:6089978..6121460hg19UCSC Ensembl
Outerchr9:6089129..6124250hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3835122
hg1935122
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154415
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006118
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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