A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115518



Internal ID21298784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89711476..89923019hg38UCSC Ensembl
Innerchr11:89444644..89656187hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38211544
hg19211544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093047
Samplessample287
Known GenesMIR5692A1, TRIM49, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64B, TRIM77
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115518
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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