A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv558n206



Internal ID22755862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1287058..1346386hg38UCSC Ensembl
chrX:1405951..1465279hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3859329
hg1959329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5428762, nsv5425650
Samples
Known GenesCSF2RA, IL3RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv558n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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