A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5300n223



Internal ID22808268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64872683..64873165hg38UCSC Ensembl
chr4:65738401..65738883hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6558011, nsv6566246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5300n223
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