A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217669



Internal ID20784709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28770271..28771431hg38UCSC Ensembl
chr10:29059200..29060360hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217669
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