A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421687



Internal ID200751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115839475..115888475hg38UCSC Ensembl
chrX:114955808..115004808hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3849001
hg1949001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421687
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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