A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416854



Internal ID196066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109556730..109556871hg38UCSC Ensembl
chrX:108799959..108800100hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv577n206
Supporting Variantsnssv17741931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416854
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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