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nsv6536838

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:394

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 17 studies. See in: genome view    
    Submitted genomic45,868,659-45,869,052Question Mark
    Overlapping variant regions from other studies: 112 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):44,497,298-44,497,691Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6536838Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2045,868,65945,869,052
    nsv6536838RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2044,497,29844,497,691

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18068364deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18068364Submitted genomicNC_000020.11:g.458
    68659_45869052del
    GRCh38 (hg38)NC_000020.11Chr2045,868,65945,869,052
    nssv18068364RemappedPerfectNC_000020.10:g.444
    97298_44497691del
    GRCh37.p13First PassNC_000020.10Chr2044,497,29844,497,691

    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)
    nssv18068364<0.001134112
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