A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3103n223



Internal ID22806071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39004848..39006096hg38UCSC Ensembl
chr17:37161101..37162349hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6582656, nsv6576839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3103n223
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