A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554813



Internal ID15995536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55592737..55692619hg38UCSC Ensembl
Innerchr11:55360213..55460095hg19UCSC Ensembl
Innerchr11:55116789..55216671hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3899883
hg1999883
hg1899883
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1906n54
Supporting Variantsnssv775188, nssv775192, nssv775191, nssv775190, nssv775189, nssv775193, nssv1174655
Samples1787431166_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)nsv554813
Frequency
Sample Size17421
Observed Gain1
Observed Loss6
Observed Complex0
Frequencyn/a


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