A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6109n223



Internal ID22809077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29790274..29960754hg38UCSC Ensembl
chr6:29758051..29928531hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38170481
hg19170481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6396432, nsv6400336, nsv6396925, nsv6397579, nsv6413276, nsv6415531, nsv6403866, nsv6406620
Samples
Known GenesHCG4, HCG4B, HLA-A, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6109n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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