A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233095



Internal ID20800135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68449040..68449856hg38UCSC Ensembl
chr10:70208797..70209613hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581040
Supporting Variants
Samples
Known GenesDNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233095
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