A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528209



Internal ID15108816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109952819..110202456hg38UCSC Ensembl
Innerchr9:112715099..112964736hg19UCSC Ensembl
Innerchr9:111754920..112004557hg18UCSC Ensembl
Innerchr9:109794654..110044291hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38249638
hg19249638
hg18249638
hg17249638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv494n21
Supporting Variantsnssv704770
Samples
Known GenesAKAP2, C9orf152, PALM2-AKAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528209
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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