A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665389



Internal ID21613694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114076028..114079947hg38UCSC Ensembl
chrX:113319218..113323145hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383920
hg193928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165030
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665389
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer