A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899655



Internal ID547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:247762807..247858974hg38UCSC Ensembl
chr1:247926109..248022276hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3896168
hg1996168
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558819
Supporting Variants
Samples
Known GenesOR11L1, OR14A16, TRIM58
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899655
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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