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nsv6526484

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,214

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 26 studies. See in: genome view    
    Submitted genomic11,336,738-11,341,951Question Mark
    Overlapping variant regions from other studies: 106 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):11,447,414-11,452,627Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6526484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1911,336,73811,341,951
    nsv6526484RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1911,447,41411,452,627

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18044998deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18044998Submitted genomicNC_000019.10:g.113
    36738_11341951del
    GRCh38 (hg38)NC_000019.10Chr1911,336,73811,341,951
    nssv18044998RemappedPerfectNC_000019.9:g.1144
    7414_11452627del
    GRCh37.p13First PassNC_000019.9Chr1911,447,41411,452,627

    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)
    nssv18044998<0.001239124
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