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nsv6962203

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,446

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 26 studies. See in: genome view    
    Submitted genomic64,461,768-64,464,213Question Mark
    Overlapping variant regions from other studies: 96 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):64,928,486-64,930,931Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962203Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,461,76864,464,213
    nsv6962203RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1464,928,48664,930,931

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18388554deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18388554Submitted genomicNC_000014.9:g.6446
    1768_64464213del
    GRCh38 (hg38)NC_000014.9Chr1464,461,76864,464,213
    nssv18388554RemappedPerfectNC_000014.8:g.6492
    8486_64930931del
    GRCh37.p13First PassNC_000014.8Chr1464,928,48664,930,931

    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)
    nssv183885544e-061274448
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