A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668659



Internal ID15058625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117241810..117285836hg38UCSC Ensembl
Innerchr11:117112526..117156552hg19UCSC Ensembl
Innerchr11:116617736..116661762hg18UCSC Ensembl
Innerchr11:116617736..116661762hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3844027
hg1944027
hg1844027
hg1744027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516483
Supporting Variants
Samples
Known GenesBACE1, RNF214
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668659
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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