A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841239



Internal ID22616174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118774128..118786389hg38UCSC Ensembl
chr5:118109823..118122084hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3812262
hg1912262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841239
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