A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598484



Internal ID20971555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32619665..32623454hg38UCSC Ensembl
chr20:31207467..31211256hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383790
hg193790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598484
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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