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nsv6992910

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38,513

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 261 SVs from 39 studies. See in: genome view    
    Submitted genomic75,883,689-75,922,201Question Mark
    Overlapping variant regions from other studies: 261 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):73,879,770-73,918,282Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992910Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,883,68975,922,201
    nsv6992910RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,879,77073,918,282

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18415286deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18415286Submitted genomicNC_000017.11:g.758
    83689_75922201del
    GRCh38 (hg38)NC_000017.11Chr1775,883,68975,922,201
    nssv18415286RemappedPerfectNC_000017.10:g.738
    79770_73918282del
    GRCh37.p13First PassNC_000017.10Chr1773,879,77073,918,282

    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)
    nssv184152864e-061276230
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