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nsv6511679

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:438

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 23 studies. See in: genome view    
    Submitted genomic41,572,564-41,573,001Question Mark
    Overlapping variant regions from other studies: 99 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):41,864,762-41,865,199Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6511679Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1541,572,56441,573,001
    nsv6511679RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,864,76241,865,199

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18023895deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18023895Submitted genomicNC_000015.10:g.415
    72564_41573001del
    GRCh38 (hg38)NC_000015.10Chr1541,572,56441,573,001
    nssv18023895RemappedPerfectNC_000015.9:g.4186
    4762_41865199del
    GRCh37.p13First PassNC_000015.9Chr1541,864,76241,865,199

    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)
    nssv18023895<0.0011828134
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