A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741258



Internal ID164924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87234328..87240361hg38UCSC Ensembl
chrX:86489331..86495364hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg386034
hg196034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741258
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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