A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154508



Internal ID22085013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69482739..69503518hg38UCSC Ensembl
Outerchr9:69476351..69505204hg38UCSC Ensembl
Innerchr9:72097655..72118434hg19UCSC Ensembl
Outerchr9:72091267..72120120hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3828854
hg1928854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv301n97
Supporting Variantsnssv4006656
Samples
Known GenesAPBA1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154508
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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