A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598467



Internal ID20971538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52916789..52916875hg38UCSC Ensembl
chr20:51533328..51533414hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598467
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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