A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540556



Internal ID315305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94512696..94512809hg38UCSC Ensembl
chrX:93767695..93767808hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540556
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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