A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596050



Internal ID20969121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63950009..63953818hg38UCSC Ensembl
chr20:62581362..62585171hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383810
hg193810
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254096
Samples
Known GenesUCKL1, UCKL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596050
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer