A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6188n223



Internal ID22809156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54942801..55007800hg38UCSC Ensembl
chr6:54807599..54872598hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3865000
hg1965000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6412264, nsv6406071
Samples
Known GenesFAM83B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6188n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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