A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414238



Internal ID193524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114366090..114367456hg38UCSC Ensembl
chrX:113600543..113601909hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381367
hg191367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414238
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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