A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112596



Internal ID21295862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:109046536..109076910hg38UCSC Ensembl
Innerchr11:108917263..108947637hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3830375
hg1930375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093252
Samplessample370
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112596
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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