A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518092



Internal ID15445385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20406956..20420100hg38UCSC Ensembl
Innerchr5:20407065..20420209hg19UCSC Ensembl
Innerchr5:20442822..20455966hg18UCSC Ensembl
Innerchr5:20442822..20455966hg17UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3813145
hg1913145
hg1813145
hg1713145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695504
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518092
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