A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874198



Internal ID22649149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29310233..29317735hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387503
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1299n209
Supporting Variantsnssv17483988, nssv17483987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874198
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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