A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6416n223



Internal ID22809384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135180201..135184100hg38UCSC Ensembl
chr6:135501339..135505238hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6600592, nsv6611528
Samples
Known GenesMYB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6416n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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