A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1425n223



Internal ID22804393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14222084..14223139hg38UCSC Ensembl
chr12:14375018..14376073hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6587528, nsv6593545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1425n223
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