A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417867



Internal ID197052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110487647..110487801hg38UCSC Ensembl
chrX:109730875..109731029hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417867
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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