A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146404



Internal ID345609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30699000..30761000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3862001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146404
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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