A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252956



Internal ID20819996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25928074..25928851hg38UCSC Ensembl
chr21:27300386..27301163hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598145
Supporting Variants
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252956
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