A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554903



Internal ID15995626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55698436hg38UCSC Ensembl
Innerchr11:55371021..55465912hg19UCSC Ensembl
Innerchr11:55127597..55222488hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3894892
hg1994892
hg1894892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1916n54
Supporting Variantsnssv1175380
Samples1780854537_A
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)nsv554903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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