A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255794



Internal ID20822835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16297807..16300469hg38UCSC Ensembl
chr2:16479075..16481737hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255794
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