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nsv6471461

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,707

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 15 studies. See in: genome view    
    Submitted genomic124,808,783-124,811,489Question Mark
    Overlapping variant regions from other studies: 151 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):124,678,679-124,681,385Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6471461Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,808,783124,811,489
    nsv6471461RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,678,679124,681,385

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17987843deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17987843Submitted genomicNC_000011.10:g.124
    808783_124811489de
    l
    GRCh38 (hg38)NC_000011.10Chr11124,808,783124,811,489
    nssv17987843RemappedPerfectNC_000011.9:g.1246
    78679_124681385del
    GRCh37.p13First PassNC_000011.9Chr11124,678,679124,681,385

    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)
    nssv17987843<0.001138974
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