A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518238



Internal ID15445531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176471198..176494720hg38UCSC Ensembl
Innerchr3:176188986..176212508hg19UCSC Ensembl
Innerchr3:177671680..177695202hg18UCSC Ensembl
Innerchr3:177671688..177695210hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3823523
hg1923523
hg1823523
hg1723523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695670
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518238
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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