A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553288



Internal ID16340697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5738876..5788581hg38UCSC Ensembl
Innerchr11:5760106..5809811hg19UCSC Ensembl
Innerchr11:5716682..5766387hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3849706
hg1949706
hg1849706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1612n54
Supporting Variantsnssv765881
Samples
Known GenesOR52N1, OR52N4, OR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553288
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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