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nsv6323203

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 22 studies. See in: genome view    
    Submitted genomic197,929,201-197,931,500Question Mark
    Overlapping variant regions from other studies: 143 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):197,898,331-197,900,630Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6323203Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1197,929,201197,931,500
    nsv6323203RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1197,898,331197,900,630

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18056177deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18056177Submitted genomicNC_000001.11:g.197
    929201_197931500de
    l
    GRCh38 (hg38)NC_000001.11Chr1197,929,201197,931,500
    nssv18056177RemappedPerfectNC_000001.10:g.197
    898331_197900630de
    l
    GRCh37.p13First PassNC_000001.10Chr1197,898,331197,900,630

    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)
    nssv18056177<0.001438748
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