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nsv6724893

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:381

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 28 studies. See in: genome view    
    Submitted genomic47,989,675-47,990,055Question Mark
    Overlapping variant regions from other studies: 115 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):47,991,692-47,992,072Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6724893Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr447,989,67547,990,055
    nsv6724893RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr447,991,69247,992,072

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18496338deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18496338Submitted genomicNC_000004.12:g.479
    89675_47990055del
    GRCh38 (hg38)NC_000004.12Chr447,989,67547,990,055
    nssv18496338RemappedPerfectNC_000004.11:g.479
    91692_47992072del
    GRCh37.p13First PassNC_000004.11Chr447,991,69247,992,072

    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)
    nssv184963380.0112834255518
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