A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262855



Internal ID20829895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69215946..69216105hg38UCSC Ensembl
chr3:69265097..69265256hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538499
Supporting Variants
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262855
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