A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515489



Internal ID15443336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5841302..5913873hg38UCSC Ensembl
Innerchr11:5862532..5935103hg19UCSC Ensembl
Innerchr11:5819108..5891679hg18UCSC Ensembl
Innerchr11:5819108..5891679hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3872572
hg1972572
hg1872572
hg1772572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678292, nssv653296, nssv680107, nssv690559, nssv691247
Samples
Known GenesOR52E4, OR52E6, OR52E8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515489
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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