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nsv6994592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:317

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 40 studies. See in: genome view    
    Submitted genomic77,992,217-77,992,533Question Mark
    Overlapping variant regions from other studies: 147 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):75,988,298-75,988,614Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6994592Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1777,992,21777,992,533
    nsv6994592RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1775,988,29875,988,614

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413328deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413328Submitted genomicNC_000017.11:g.779
    92217_77992533del
    GRCh38 (hg38)NC_000017.11Chr1777,992,21777,992,533
    nssv18413328RemappedPerfectNC_000017.10:g.759
    88298_75988614del
    GRCh37.p13First PassNC_000017.10Chr1775,988,29875,988,614

    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)
    nssv184133280.541126742235842
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