A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv571n206



Internal ID22755875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76579925..76602886hg38UCSC Ensembl
chrX:75800318..75823295hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3822962
hg1922978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5419810, nsv5425431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv571n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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