A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv437n223



Internal ID22803405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169446404..169447313hg38UCSC Ensembl
chr1:169415642..169416551hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6546312, nsv6545422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv437n223
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