A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553123



Internal ID16340532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3142423..3159855hg38UCSC Ensembl
Innerchr11:3163653..3181085hg19UCSC Ensembl
Innerchr11:3120229..3137661hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3817433
hg1917433
hg1817433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764550
Samples
Known GenesOSBPL5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553123
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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