A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554812



Internal ID15995535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55592737..55685447hg38UCSC Ensembl
Innerchr11:55360213..55452923hg19UCSC Ensembl
Innerchr11:55116789..55209499hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3892711
hg1992711
hg1892711
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1906n54
Supporting Variantsnssv775183, nssv775181, nssv775184, nssv775186, nssv775187, nssv775179, nssv775182, nssv775185, nssv775180
Samples
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)nsv554812
Frequency
Sample Size17421
Observed Gain4
Observed Loss5
Observed Complex0
Frequencyn/a


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