A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519284



Internal ID15446577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47173502..47180971hg38UCSC Ensembl
Innerchr15:47465699..47473168hg19UCSC Ensembl
Innerchr15:45252991..45260460hg18UCSC Ensembl
Innerchr15:45252991..45260460hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg387470
hg197470
hg187470
hg177470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696765
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519284
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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