A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv48n223



Internal ID22803016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11928601..11933600hg38UCSC Ensembl
chr1:11988658..11993657hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6324746, nsv6317625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv48n223
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