A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2293n209



Internal ID22828368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109653483..109658962hg38UCSC Ensembl
chrX:108896712..108902191hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385480
hg195480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5868944, nsv5869115
Samples
Known GenesACSL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2293n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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