A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045742



Internal ID21955001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22262141..22264345hg38UCSC Ensembl
chr20:22242779..22244983hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg382205
hg192205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045742
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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