A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252212



Internal ID20819252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48856831..48857760hg38UCSC Ensembl
chr20:47473368..47474297hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252212
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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