A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278457



Internal ID20845497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65654038..65654257hg38UCSC Ensembl
chr8:66566273..66566492hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574989
Supporting Variants
Samples
Known GenesMTFR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278457
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