A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527153



Internal ID15454446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12261484..12310605hg38UCSC Ensembl
Innerchr5:12261596..12310717hg19UCSC Ensembl
Innerchr5:12314596..12363717hg18UCSC Ensembl
Innerchr5:12314596..12363717hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3849122
hg1949122
hg1849122
hg1749122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv335n21
Supporting Variantsnssv703544
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527153
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