A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2908n223



Internal ID22805876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67095695..67096323hg38UCSC Ensembl
chr16:67129598..67130226hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6581242, nsv6576318
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2908n223
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