A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554831



Internal ID15995554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55669650hg38UCSC Ensembl
Innerchr11:55367889..55437126hg19UCSC Ensembl
Innerchr11:55124465..55193702hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3869238
hg1969238
hg1869238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv775236, nssv775233, nssv775241, nssv775237, nssv775238, nssv775234, nssv775235, nssv775232, nssv775240, nssv775239
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)nsv554831
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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