A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554929



Internal ID15995652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55680970hg38UCSC Ensembl
Innerchr11:55374998..55448446hg19UCSC Ensembl
Innerchr11:55131574..55205022hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3873449
hg1973449
hg1873449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv776586, nssv776587
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)nsv554929
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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