A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243683



Internal ID20810724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69006755..69007520hg38UCSC Ensembl
chr16:69040658..69041423hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586428
Supporting Variants
Samples
Known GenesTANGO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243683
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