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nsv6976550

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 27 studies. See in: genome view    
    Submitted genomic75,001,515-75,001,610Question Mark
    Overlapping variant regions from other studies: 154 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):75,293,856-75,293,951Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6976550Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1575,001,51575,001,610
    nsv6976550RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1575,293,85675,293,951

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18398166deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18398166Submitted genomicNC_000015.10:g.750
    01515_75001610del
    GRCh38 (hg38)NC_000015.10Chr1575,001,51575,001,610
    nssv18398166RemappedPerfectNC_000015.9:g.7529
    3856_75293951del
    GRCh37.p13First PassNC_000015.9Chr1575,293,85675,293,951

    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)
    nssv183981663.1e-058252682
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