A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433089



Internal ID211816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135316457..135319587hg38UCSC Ensembl
chrX:134450383..134453513hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg383131
hg193131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433089
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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