A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146736



Internal ID345941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30628800..30642077hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3813278
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146736
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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