A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249498



Internal ID20816538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183182090..183182947hg38UCSC Ensembl
chr1:183151225..183152082hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539621
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249498
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