A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927479



Internal ID22702707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89922148..90147492hg38UCSC Ensembl
chr11:89655316..89880660hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38225345
hg19225345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365790
Samples
Known GenesMIR5692A1, NAALAD2, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, UBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927479
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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