A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599685



Internal ID20972756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10682482..10688300hg38UCSC Ensembl
chr20:10663130..10668948hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg385819
hg195819
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599685
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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