A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554829



Internal ID15995552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55655110hg38UCSC Ensembl
Innerchr11:55367889..55422586hg19UCSC Ensembl
Innerchr11:55124465..55179162hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3854698
hg1954698
hg1854698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n54
Supporting Variantsnssv775221, nssv775222, nssv775226, nssv775223, nssv775227, nssv775228, nssv775224, nssv775225
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)nsv554829
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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