A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221361



Internal ID20788401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104471183..104474027hg38UCSC Ensembl
chr10:106230941..106233785hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382845
hg192845
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221361
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