A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6456n223



Internal ID22809424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152956201..153022300hg38UCSC Ensembl
chr6:153277336..153343435hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3866100
hg1966100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6606117, nsv6607244
Samples
Known GenesFBXO5, MTRF1L, RGS17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6456n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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