A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554810



Internal ID15995533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55592737..55674892hg38UCSC Ensembl
Innerchr11:55360213..55442368hg19UCSC Ensembl
Innerchr11:55116789..55198944hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3882156
hg1982156
hg1882156
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1906n54
Supporting Variantsnssv1174647, nssv1174648, nssv1174646, nssv775171, nssv775170
SamplesHGDP00759, HGDP00511, NINDS_127
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)nsv554810
Frequency
Sample Size17421
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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