A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2084n223



Internal ID22805052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27445384..27592323hg38UCSC Ensembl
chr14:27914590..28061529hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38146940
hg19146940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6476263, nsv6479648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2084n223
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