A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925800



Internal ID22701027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89495583..89923923hg38UCSC Ensembl
chr11:89228751..89657091hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38428341
hg19428341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356578
Samples
Known GenesFOLH1B, MIR5692A1, NOX4, TRIM49, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64B, TRIM77
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925800
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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