A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522669



Internal ID15449962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11404651..11405493hg38UCSC Ensembl
Innerchr11:11426198..11427040hg19UCSC Ensembl
Innerchr11:11382774..11383616hg18UCSC Ensembl
Innerchr11:11382774..11383616hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38843
hg19843
hg18843
hg17843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706074
Samples
Known GenesGALNT18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522669
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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