A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528236



Internal ID15108843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125302778..125305585hg38UCSC Ensembl
Innerchr11:125172674..125175481hg19UCSC Ensembl
Innerchr11:124677884..124680691hg18UCSC Ensembl
Innerchr11:124677884..124680691hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382808
hg192808
hg182808
hg172808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704798
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528236
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