A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278230



Internal ID20845270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54007035..54008039hg38UCSC Ensembl
chr8:54919595..54920599hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559996
Supporting Variants
Samples
Known GenesTCEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278230
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