A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv57n199



Internal ID22802943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47833343..47898033hg38UCSC Ensembl
chr20:46462087..46526777hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3864691
hg1964691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4760798, nsv4759320, nsv4756006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv57n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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