A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv566n223



Internal ID22803534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238488418..238615200hg38UCSC Ensembl
chr1:238651718..238778500hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38126783
hg19126783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6331869, nsv6335004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv566n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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