A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1753n209



Internal ID22827828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31261615..31361743hg38UCSC Ensembl
chr6:31229392..31329520hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38100129
hg19100129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5900873, nsv5903601, nsv5900955, nsv5897473
Samples
Known GenesHLA-B, HLA-C, MIR6891
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1753n209
Frequency
Sample Size914
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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