A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553138



Internal ID16340547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3274651..3337129hg38UCSC Ensembl
Innerchr11:3295881..3358359hg19UCSC Ensembl
Innerchr11:3252457..3314935hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3862479
hg1962479
hg1862479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764601
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553138
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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