A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116523



Internal ID21299789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75972386..76153493hg38UCSC Ensembl
Innerchr11:75683430..75864537hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38181108
hg19181108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091809
Samplessample189
Known GenesUVRAG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116523
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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