A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4867n223



Internal ID22807835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48455505..48456301hg38UCSC Ensembl
chr3:48496905..48497701hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6554076, nsv6538524
Samples
Known GenesATRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4867n223
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