A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518840



Internal ID15099447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78578946..78594829hg38UCSC Ensembl
Innerchr15:78871288..78887171hg19UCSC Ensembl
Innerchr15:76658343..76674226hg18UCSC Ensembl
Innerchr15:76658343..76674226hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3815884
hg1915884
hg1815884
hg1715884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696293
Samples
Known GenesCHRNA3, CHRNA5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518840
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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