A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242820



Internal ID20809860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27948686..27949482hg38UCSC Ensembl
chr16:27960007..27960803hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589185
Supporting Variants
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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