A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv511n223



Internal ID22803479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202984711..202986358hg38UCSC Ensembl
chr1:202953839..202955486hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381648
hg191648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6537317, nsv6541373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv511n223
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