A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2267n209



Internal ID22828342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2448174..2470962hg38UCSC Ensembl
chrX:2366215..2389003hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3822789
hg1922789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5868518, nsv5880541
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2267n209
Frequency
Sample Size914
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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