A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554923



Internal ID15995646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55685447hg38UCSC Ensembl
Innerchr11:55373973..55452923hg19UCSC Ensembl
Innerchr11:55130549..55209499hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3878951
hg1978951
hg1878951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv776575, nssv776563, nssv776566, nssv776577, nssv776576, nssv776573, nssv776564, nssv776572, nssv776571, nssv776565, nssv776562, nssv776574, nssv776569, nssv776570, nssv776568, nssv776567
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)nsv554923
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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