A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884839



Internal ID22659823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49734146..49739886hg38UCSC Ensembl
chr18:47260516..47266256hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg385741
hg195741
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884839
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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