A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563457



Internal ID336391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135158636..135213909hg38UCSC Ensembl
chrX:134292561..134347840hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3855274
hg1955280
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742465
Samples
Known GenesCXorf48
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563457
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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