A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524569



Internal ID15451862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59374793..59420228hg38UCSC Ensembl
Innerchr15:59666992..59712427hg19UCSC Ensembl
Innerchr15:57454284..57499719hg18UCSC Ensembl
Innerchr15:57454284..57499719hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3845436
hg1945436
hg1845436
hg1745436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700524
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524569
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer