A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414144



Internal ID193429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153769676..153769746hg38UCSC Ensembl
chrX:153035131..153035201hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738090
Samples
Known GenesPLXNB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414144
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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