A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957917



Internal ID22733011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:28840893..29152529hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38311637
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957917
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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