A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599736



Internal ID20972807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50443548..50444839hg38UCSC Ensembl
chr20:49060085..49061376hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381292
hg191292
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4483n223
Supporting Variantsnssv18252598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599736
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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