A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523104



Internal ID15450397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24793064..24810155hg38UCSC Ensembl
Innerchr15:25038211..25055302hg19UCSC Ensembl
Innerchr15:22589304..22606395hg18UCSC Ensembl
Innerchr15:22589304..22606395hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3817092
hg1917092
hg1817092
hg1717092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698800
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523104
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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