A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv568n223



Internal ID22803536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239101306..239107100hg38UCSC Ensembl
chr1:239264606..239270400hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg385795
hg195795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6323764, nsv6333112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv568n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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