A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4807n223



Internal ID22807775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17972301..18000300hg38UCSC Ensembl
chr3:18013793..18041792hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3828000
hg1928000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6367814, nsv6358827
Samples
Known GenesLOC339862
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4807n223
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