A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875836



Internal ID22650795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:28624155..28632101hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387947
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1287n209
Supporting Variantsnssv17483956, nssv17483955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875836
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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