A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671133



Internal ID21619438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154549471..154555683hg38UCSC Ensembl
chrX:153777686..153783898hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386213
hg196213
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166288
SamplesNA12878
Known GenesIKBKG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671133
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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