A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554896



Internal ID15995619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55677392hg38UCSC Ensembl
Innerchr11:55371021..55444868hg19UCSC Ensembl
Innerchr11:55127597..55201444hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3873848
hg1973848
hg1873848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv776024, nssv1175194, nssv1175193, nssv776025, nssv1175195
SamplesHGDP00637, HGDP00047, NINDS_232
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)nsv554896
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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