A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947580



Internal ID22723087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29968168..30009970hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3841803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947580
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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