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nsv6348207

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:667

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 19 studies. See in: genome view    
    Submitted genomic46,627,575-46,628,241Question Mark
    Overlapping variant regions from other studies: 128 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):46,854,714-46,855,380Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6348207Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr246,627,57546,628,241
    nsv6348207RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr246,854,71446,855,380

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18090569deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18090569Submitted genomicNC_000002.12:g.466
    27575_46628241del
    GRCh38 (hg38)NC_000002.12Chr246,627,57546,628,241
    nssv18090569RemappedPerfectNC_000002.11:g.468
    54714_46855380del
    GRCh37.p13First PassNC_000002.11Chr246,854,71446,855,380

    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)
    nssv18090569<0.001236354
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