A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520375



Internal ID15447668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56902354..56936567hg38UCSC Ensembl
Innerchr11:56669830..56704042hg19UCSC Ensembl
Innerchr11:56426406..56460618hg18UCSC Ensembl
Innerchr11:56426406..56460618hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3834214
hg1934213
hg1834213
hg1734213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675144, nssv663334, nssv700910
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520375
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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