A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1612n54



Internal ID22769507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5738876..5788581hg38UCSC Ensembl
chr11:5760106..5809811hg19UCSC Ensembl
chr11:5716682..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 Variants
Supporting Variantsnsv553295, nsv553292, nsv553288
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)dgv1612n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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