A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3795n223



Internal ID22806763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14530114..14531082hg38UCSC Ensembl
chr2:14670238..14671206hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6549109, nsv6551980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3795n223
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