A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3330n223



Internal ID22806298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26590885..26591949hg38UCSC Ensembl
chr18:24170849..24171913hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6585393, nsv6593338
Samples
Known GenesKCTD1, MIR8057
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3330n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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