A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842123



Internal ID22617058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171988888..171995665hg38UCSC Ensembl
chr5:171415892..171422669hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg386778
hg196778
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497698
Samples
Known GenesFBXW11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842123
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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