A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116653



Internal ID21299919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22632668..22645021hg38UCSC Ensembl
Innerchr11:22654214..22666567hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3812354
hg1912354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090032
Samplessample29
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116653
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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