A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848416



Internal ID22623351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:457412..464511hg38UCSC Ensembl
chr8:407412..414511hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506731, nssv17509240
Samples
Known GenesFBXO25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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