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nstd217 (Zhang et al. 2022)

Organism:
Human
Study Type:
Somatic
Submitter:
Li-Qun Zhang
Description:
We report a rare interlocus recombination between HLA-A and HLA-H, which was analyzed using next generation sequencing and nanopore sequencing.In the sample, the genotypes of HLA-A, B, C, DRB1, and DQB1 were firstly determined using the methods of sequence-specific primer, sequence-specific oligonucleotide, Sanger’s sequencing, and NGS; however, HLA-A could not be phased. Nanopore sequencing was finally utilized to distinguish the sequence of the novel allele.The novel HLA-A*11:335 allele was identified as an interlocus recombination involving HLA-A*11:01:01:01/126 and HLA-H*02:07/14/18 alleles; this was mainly achieved by nanopore sequencing. See Variant Summary counts for nstd217 in dbVar Variant Summary.
Publication(s):
Zhang et al. 2022

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_000006.12Chr611SubmittedNC_000006.12
Sequence IDChrNumber of Variant RegionsNumber of Variant CallsPlacement typeLink to graphical display
NC_000006.11Chr611RemappedNC_000006.11

Variant Region remap statusVariant Call remap status
Sequence IDChrVariant Regions on sourcePerfectGoodPassFailMultVariant Calls on sourcePerfectGoodPassFailMult
NC_000006.12Chr6110000110000

Samplesets

Number of Samplesets: 1

Name:
China Marrow Donor Program
Description:
2964 specimens were sampled (approximately 2%) from the database of recruited volunteers of the China Marrow Donor Program in 2017 and subsequently genotyped for HLA-A, B, C, DRB1, and DQB1.
Size:
2,964
Organisms:
Homo sapiens
Sampleset Phenotype(s):
None reported
  • Download Samples as CSV file
  • Samples for sampleset 1 (displaying 100 of the 2964 samples)
    Sample IDSubject ID Subject Phenotype
    17ZZ22984741700165Not reported

    Experimental Details

    Experiment IDTypeMethodAnalysisNumber of Variant Calls
    1DiscoverySequencingSequence alignment1

    Validations

    No validation data were submitted for this study.

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