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nsv6464573

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 20 studies. See in: genome view    
    Submitted genomic74,224,901-74,226,700Question Mark
    Overlapping variant regions from other studies: 85 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):73,935,946-73,937,745Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6464573Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1174,224,90174,226,700
    nsv6464573RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1173,935,94673,937,745

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17993587deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17993587Submitted genomicNC_000011.10:g.742
    24901_74226700del
    GRCh38 (hg38)NC_000011.10Chr1174,224,90174,226,700
    nssv17993587RemappedPerfectNC_000011.9:g.7393
    5946_73937745del
    GRCh37.p13First PassNC_000011.9Chr1173,935,94673,937,745

    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)
    nssv17993587<0.001139128
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