A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554856



Internal ID15995579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55684336hg38UCSC Ensembl
Innerchr11:55369626..55451812hg19UCSC Ensembl
Innerchr11:55126202..55208388hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3882187
hg1982187
hg1882187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv775704, nssv775697, nssv775696, nssv775703, nssv775701, nssv775700, nssv775702, nssv775699, nssv775706, nssv775707, nssv775705, nssv775698
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)nsv554856
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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