A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6313n223



Internal ID22809281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92859801..92898500hg38UCSC Ensembl
chr6:93569519..93608218hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3838700
hg1938700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6401671, nsv6400064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6313n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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