A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843314



Internal ID22618249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99487435..99489563hg38UCSC Ensembl
chr5:98823139..98825267hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg382129
hg192129
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500198, nssv17500197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843314
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