A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554876



Internal ID15995599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602849..55685358hg38UCSC Ensembl
Innerchr11:55370325..55452834hg19UCSC Ensembl
Innerchr11:55126901..55209410hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3882510
hg1982510
hg1882510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv775953, nssv775952, nssv775949, nssv775951, nssv775948, nssv775947, nssv775950
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)nsv554876
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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