A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965708



Internal ID22740643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:26321814..26344962hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3823149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965708
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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