A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691247



Internal ID15427899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5841302..5911882hg38UCSC Ensembl
Innerchr11:5862532..5933112hg19UCSC Ensembl
Innerchr11:5819108..5889688hg18UCSC Ensembl
Innerchr11:5819108..5889688hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3870581
hg1970581
hg1870581
hg1770581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515489
Supporting Variants
Samples
Known GenesOR52E4, OR52E6, OR52E8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691247
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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