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nstd219 (Bao et al. 2022)

Organism:
Human
Study Type:
Collection
Submitter:
Xiuqin Bao
Description:
β-thalassemia is a highly prevalent disease in Southern China and tropical and subtropical regions, which is mainly caused by point mutations in β-globin gene cluster. However, large deletions were also identified to contribute to some types of β-thalassemia. We have identified a novel 5 kb deletion in β-globin cluster in a Chinese patient by using multiplex ligation-dependent probe amplification and characterized it by single molecule real time sequencing, Gap-PCR and Sanger sequencing. The deletion was located between 5226189-5231091 in chromosome 11 (GRCh38), extending from 4 kb upstream of 5’UTR to the second intron of HBB gene. With this deletion, the patient presented with microcytosis and hypochromic red cells, as well as relatively high Hb F and Hb A2 level. Our research points out that single molecule real time sequencing is a useful tool to detect large deletions accurately. Our study widens the spectrum of deletional β-thalassemia and provides a perspective for further study of the function of β-globin cluster. See Variant Summary counts for nstd219 in dbVar Variant Summary.

Detailed Information: Download 1 Variant Region, Download 1 Variant Call, Download Both, FTP

Variant Summary

Assembly used for analysis:
Submitted: GRCh38 (hg38)
Remapped: GRCh37 (hg19)

Sequence IDChrNumber of Variant RegionsNumber of Variant CallsPlacement typeLink to graphical display
NC_000011.10Chr1111SubmittedNC_000011.10
Sequence IDChrNumber of Variant RegionsNumber of Variant CallsPlacement typeLink to graphical display
NC_000011.9Chr1111RemappedNC_000011.9

Variant Region remap statusVariant Call remap status
Sequence IDChrVariant Regions on sourcePerfectGoodPassFailMultVariant Calls on sourcePerfectGoodPassFailMult
NC_000011.10Chr11110000110000

Samplesets

Number of Samplesets: 1

Size:
1
Organisms:
Homo sapiens
Sampleset Phenotype(s):
None reported
  • Download Samples as CSV file
  • Samples for sampleset 1
    Sample IDSubject ID Subject Phenotype
    CRHCRHNot reported

    Experimental Details

    Experiment IDTypeMethodAnalysisNumber of Variant Calls
    1DiscoverySequencingSequence alignment1

    Validations

    No validation data were submitted for this study.

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