A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2294n209



Internal ID22828369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115307786..115309957hg38UCSC Ensembl
chrX:114542351..114544522hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg382172
hg192172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5880313, nsv5881297, nsv5880467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2294n209
Frequency
Sample Size914
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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