A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840881



Internal ID22615816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107971285..107973014hg38UCSC Ensembl
chr5:107306986..107308715hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg381730
hg191730
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493003
Samples
Known GenesFBXL17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840881
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer