A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520880



Internal ID15101487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11563899..11576994hg38UCSC Ensembl
Innerchr3:11605373..11618468hg19UCSC Ensembl
Innerchr3:11580373..11593468hg18UCSC Ensembl
Innerchr3:11580373..11593468hg17UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3813096
hg1913096
hg1813096
hg1713096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676873, nssv677738
Samples
Known GenesVGLL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520880
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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