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nsv6986244

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,517

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 222 SVs from 34 studies. See in: genome view    
    Submitted genomic75,583,747-75,587,263Question Mark
    Overlapping variant regions from other studies: 222 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):73,579,828-73,583,344Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6986244Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,583,74775,587,263
    nsv6986244RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,579,82873,583,344

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18415257deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18415257Submitted genomicNC_000017.11:g.755
    83747_75587263del
    GRCh38 (hg38)NC_000017.11Chr1775,583,74775,587,263
    nssv18415257RemappedPerfectNC_000017.10:g.735
    79828_73583344del
    GRCh37.p13First PassNC_000017.10Chr1773,579,82873,583,344

    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)
    nssv184152574e-061275958
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