A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554800



Internal ID15995523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55315958..55928509hg38UCSC Ensembl
Innerchr11:55083434..55695985hg19UCSC Ensembl
Innerchr11:54840010..55452561hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38612552
hg19612552
hg18612552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1905n54
Supporting Variantsnssv775160
Samples
Known GenesOR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2, OR5W2, TRIM51
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554800
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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