A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6038n223



Internal ID22809006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:245801..412500hg38UCSC Ensembl
chr6:245801..412500hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38166700
hg19166700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6399475, nsv6414891, nsv6405822, nsv6399836, nsv6398778, nsv6396300, nsv6399088
Samples
Known GenesDUSP22, IRF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6038n223
Frequency
Sample Size19652
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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