A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6107n223



Internal ID22809075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29720392..29993550hg38UCSC Ensembl
chr6:29688169..29961327hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38273159
hg19273159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6407238, nsv6398946, nsv6407168
Samples
Known GenesHCG4, HCG4B, HCG9, HLA-A, HLA-F, HLA-F-AS1, HLA-G, HLA-H, IFITM4P, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6107n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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