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nsv6474230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:522

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 160 SVs from 44 studies. See in: genome view    
    Submitted genomic55,982,098-55,982,619Question Mark
    Overlapping variant regions from other studies: 163 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):55,749,574-55,750,095Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6474230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1155,982,09855,982,619
    nsv6474230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1155,749,57455,750,095

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17992374deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17992374Submitted genomicNC_000011.10:g.559
    82098_55982619del
    GRCh38 (hg38)NC_000011.10Chr1155,982,09855,982,619
    nssv17992374RemappedPerfectNC_000011.9:g.5574
    9574_55750095del
    GRCh37.p13First PassNC_000011.9Chr1155,749,57455,750,095

    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)
    nssv17992374<0.0013237444
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