A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554842



Internal ID15995565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55639688hg38UCSC Ensembl
Innerchr11:55369626..55407164hg19UCSC Ensembl
Innerchr11:55126202..55163740hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3837539
hg1937539
hg1837539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1911n54
Supporting Variantsnssv775665, nssv775666, nssv775664, nssv775663
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554842
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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