A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957643



Internal ID22732757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171893421..171893421hg38UCSC Ensembl
chr5:171320425..171320425hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412454
Samples
Known GenesFBXW11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957643
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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