A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146351



Internal ID345556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44881801..44884572hg38UCSC Ensembl
chr20:43510442..43513213hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382772
hg192772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146351
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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