A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221148



Internal ID20788188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107837960..108887560hg38UCSC Ensembl
chr10:109597718..110647318hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381049601
hg191049601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575989
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221148
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