A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248841



Internal ID20815881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179908872..179909398hg38UCSC Ensembl
chr1:179878007..179878533hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547675
Supporting Variants
Samples
Known GenesTOR1AIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248841
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer