A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2292n209



Internal ID22828367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103523733..103554101hg38UCSC Ensembl
chrX:102778661..102809029hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3830369
hg1930369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5872000, nsv5871910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2292n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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