A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1706n223



Internal ID22804674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118693238..118695166hg38UCSC Ensembl
chr12:119131043..119132971hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381929
hg191929
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6584739, nsv6575906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1706n223
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