A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154474



Internal ID22084979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28491681..28509747hg38UCSC Ensembl
Outerchr9:28486254..28512124hg38UCSC Ensembl
Innerchr9:28491679..28509745hg19UCSC Ensembl
Outerchr9:28486252..28512122hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3825871
hg1925871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007038
Samples
Known GenesLINGO2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154474
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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