A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517849



Internal ID15098456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58361580..58496708hg38UCSC Ensembl
Innerchr11:58129053..58264181hg19UCSC Ensembl
Innerchr11:57885629..58020757hg18UCSC Ensembl
Innerchr11:57885629..58020757hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38135129
hg19135129
hg18135129
hg17135129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695254
Samples
Known GenesOR5B12, OR5B2, OR5B3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517849
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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