A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1620n54



Internal ID22769515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5765554..5788000hg38UCSC Ensembl
chr11:5786784..5809230hg19UCSC Ensembl
chr11:5743360..5765806hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3822447
hg1922447
hg1822447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553342, nsv553337, nsv553338, nsv553343, nsv553335, nsv553341, nsv553340, nsv553330, nsv553334
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1620n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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