A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843507



Internal ID22618442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82465540..82471906hg38UCSC Ensembl
chr5:81761359..81767725hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg386367
hg196367
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843507
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