A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526267



Internal ID15106874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117815479..117837222hg38UCSC Ensembl
Innerchr11:117686194..117707937hg19UCSC Ensembl
Innerchr11:117191404..117213147hg18UCSC Ensembl
Innerchr11:117191404..117213147hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3821744
hg1921744
hg1821744
hg1721744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702540
Samples
Known GenesFXYD2, FXYD6, FXYD6-FXYD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526267
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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