A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554886



Internal ID15995609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55639307hg38UCSC Ensembl
Innerchr11:55371021..55406783hg19UCSC Ensembl
Innerchr11:55127597..55163359hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3835763
hg1935763
hg1835763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1911n54
Supporting Variantsnssv775979, nssv775978, nssv775976, nssv775977
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554886
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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