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nsv6535499

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,924

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 34 studies. See in: genome view    
    Submitted genomic18,271,864-18,275,787Question Mark
    Overlapping variant regions from other studies: 129 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):18,382,674-18,386,597Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6535499Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1918,271,86418,275,787
    nsv6535499RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1918,382,67418,386,597

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18045080deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18045080Submitted genomicNC_000019.10:g.182
    71864_18275787del
    GRCh38 (hg38)NC_000019.10Chr1918,271,86418,275,787
    nssv18045080RemappedPerfectNC_000019.9:g.1838
    2674_18386597del
    GRCh37.p13First PassNC_000019.9Chr1918,382,67418,386,597

    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)
    nssv18045080<0.001138902
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