A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554859



Internal ID15995582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55685358hg38UCSC Ensembl
Innerchr11:55369626..55452834hg19UCSC Ensembl
Innerchr11:55126202..55209410hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3883209
hg1983209
hg1883209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv775739, nssv775724, nssv775726, nssv775743, nssv775741, nssv775727, nssv775733, nssv775722, nssv775740, nssv775736, nssv775730, nssv775738, nssv775728, nssv775723, nssv775742, nssv775721, nssv775734, nssv775725, nssv775731, nssv775729, nssv775735, nssv775737, nssv775732
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554859
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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