A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5629n223



Internal ID22808597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6606587..6607311hg38UCSC Ensembl
chr5:6606700..6607424hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6561304, nsv6568276
Samples
Known GenesNSUN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5629n223
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