A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257882



Internal ID20824922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205846380..205847135hg38UCSC Ensembl
chr2:206711104..206711859hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542484
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257882
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