A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518770



Internal ID15446063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26210454..26223932hg38UCSC Ensembl
Innerchr5:26210563..26224041hg19UCSC Ensembl
Innerchr5:26246320..26259798hg18UCSC Ensembl
Innerchr5:26246320..26259798hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3813479
hg1913479
hg1813479
hg1713479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696220
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518770
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