A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1528n223



Internal ID22804496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41081556..41093457hg38UCSC Ensembl
chr12:41475358..41487259hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3811902
hg1911902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6462640, nsv6456209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1528n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer