A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672068



Internal ID21620373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154347666..154384612hg38UCSC Ensembl
chrX:153576034..153612972hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3836947
hg1936939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166283
SamplesHG00513
Known GenesEMD, FLNA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672068
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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