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nsv6887088

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,910

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 29 studies. See in: genome view    
    Submitted genomic5,515,727-5,524,636Question Mark
    Overlapping variant regions from other studies: 139 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):5,557,690-5,566,599Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6887088Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr105,515,7275,524,636
    nsv6887088RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr105,557,6905,566,599

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18337369deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18337369Submitted genomicNC_000010.11:g.551
    5727_5524636del
    GRCh38 (hg38)NC_000010.11Chr105,515,7275,524,636
    nssv18337369RemappedPerfectNC_000010.10:g.555
    7690_5566599del
    GRCh37.p13First PassNC_000010.10Chr105,557,6905,566,599

    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)
    nssv183373694e-061275900
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