A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154472



Internal ID22084977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27994936..28013476hg38UCSC Ensembl
Outerchr9:27992873..28015472hg38UCSC Ensembl
Innerchr9:27994934..28013474hg19UCSC Ensembl
Outerchr9:27992871..28015470hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3822600
hg1922600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007026
Samples
Known GenesLINGO2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154472
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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