A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6117n223



Internal ID22809085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29886014..29952661hg38UCSC Ensembl
chr6:29853791..29920438hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3866648
hg1966648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6413158, nsv6408681, nsv6398324, nsv6404865, nsv6401821
Samples
Known GenesHCG4B, HLA-A, HLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6117n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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