A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518046



Internal ID15445339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69919567..69923743hg38UCSC Ensembl
Innerchr15:70211906..70216082hg19UCSC Ensembl
Innerchr15:67998960..68003136hg18UCSC Ensembl
Innerchr15:67998960..68003136hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384177
hg194177
hg184177
hg174177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695457
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518046
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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