A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1915n223



Internal ID22804883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73067968..73068858hg38UCSC Ensembl
chr13:73642106..73642996hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6590146, nsv6577166
Samples
Known GenesKLF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1915n223
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