A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518422



Internal ID15099029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112235008..112242230hg38UCSC Ensembl
Innerchr9:114997288..115004510hg19UCSC Ensembl
Innerchr9:114037109..114044331hg18UCSC Ensembl
Innerchr9:112076843..112084065hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg387223
hg197223
hg187223
hg177223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695857
Samples
Known GenesMIR3134, PTBP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518422
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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