A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554891



Internal ID15995614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55655110hg38UCSC Ensembl
Innerchr11:55371021..55422586hg19UCSC Ensembl
Innerchr11:55127597..55179162hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3851566
hg1951566
hg1851566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n54
Supporting Variantsnssv776002, nssv775997, nssv776000, nssv776001, nssv775998, nssv775999, nssv775996
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554891
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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