A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598087



Internal ID20971158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56650873..56652477hg38UCSC Ensembl
chr20:55225929..55227533hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381605
hg191605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598087
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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