A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2281n209



Internal ID22828356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:67406139..67415462hg38UCSC Ensembl
chrX:66625981..66635304hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg389324
hg199324
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5969072, nsv5974192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2281n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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