A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553158



Internal ID16340567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4366530..4393849hg38UCSC Ensembl
Innerchr11:4387760..4415079hg19UCSC Ensembl
Innerchr11:4344336..4371655hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3827320
hg1927320
hg1827320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1582n54
Supporting Variantsnssv764647
Samples
Known GenesOR52B4, TRIM21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553158
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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