A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6110n223



Internal ID22809078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29793191..29986400hg38UCSC Ensembl
chr6:29760968..29954177hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38193210
hg19193210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6402572, nsv6397804, nsv6405513, nsv6395658, nsv6415275, nsv6398733
Samples
Known GenesHCG4B, HCG9, HLA-A, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6110n223
Frequency
Sample Size19652
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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