A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5543333



Internal ID317598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97570141..97570224hg38UCSC Ensembl
chrX:96825140..96825223hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737103
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5543333
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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