A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1302n223



Internal ID22804270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106058182..106058578hg38UCSC Ensembl
chr11:105928909..105929305hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577508, nsv6588632
Samples
Known GenesKBTBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1302n223
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