A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365790



Internal ID22591459
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 StatusS
Merged Variantsnsv5927479
Supporting Variants
Samples
Known GenesMIR5692A1, NAALAD2, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, UBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365790
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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