A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554922



Internal ID15995645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55679951hg38UCSC Ensembl
Innerchr11:55373973..55447427hg19UCSC Ensembl
Innerchr11:55130549..55204003hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3873455
hg1973455
hg1873455
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1915n54
Supporting Variantsnssv776547, nssv776549, nssv776555, nssv776543, nssv776546, nssv776561, nssv776550, nssv776554, nssv776559, nssv776545, nssv776558, nssv776557, nssv776542, nssv776553, nssv776556, nssv776544, nssv776560, nssv776551, nssv776548, nssv776552
Samples
Known GenesOR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554922
Frequency
Sample Size17421
Observed Gain5
Observed Loss15
Observed Complex0
Frequencyn/a


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