A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598267



Internal ID20971338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46753692..46754395hg38UCSC Ensembl
chr20:45382331..45383034hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598267
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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