A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553177



Internal ID16340586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4785642..4850276hg38UCSC Ensembl
Innerchr11:4806872..4871506hg19UCSC Ensembl
Innerchr11:4763448..4828082hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3864635
hg1964635
hg1864635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1588n54
Supporting Variantsnssv764671
Samples
Known GenesOR51F2, OR51S1, OR52R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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