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nsv6717423

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,417

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Submitted genomic35,150,622-35,157,038Question Mark
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):35,192,114-35,198,530Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6717423Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr335,150,62235,157,038
    nsv6717423RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr335,192,11435,198,530

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18480731deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18480731Submitted genomicNC_000003.12:g.351
    50622_35157038del
    GRCh38 (hg38)NC_000003.12Chr335,150,62235,157,038
    nssv18480731RemappedPerfectNC_000003.11:g.351
    92114_35198530del
    GRCh37.p13First PassNC_000003.11Chr335,192,11435,198,530

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv184807314e-061276160
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