A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885349



Internal ID22660333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56354718..56359321hg38UCSC Ensembl
chr18:54021949..54026552hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg384604
hg194604
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885349
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