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nsv6780091

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134,394

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 503 SVs from 64 studies. See in: genome view    
    Submitted genomic163,413,470-163,547,863Question Mark
    Overlapping variant regions from other studies: 503 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):162,840,476-162,974,869Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6780091Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5163,413,470163,547,863
    nsv6780091RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5162,840,476162,974,869

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18508803deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18508803Submitted genomicNC_000005.10:g.163
    413470_163547863de
    l
    GRCh38 (hg38)NC_000005.10Chr5163,413,470163,547,863
    nssv18508803RemappedPerfectNC_000005.9:g.1628
    40476_162974869del
    GRCh37.p13First PassNC_000005.9Chr5162,840,476162,974,869

    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)
    nssv185088034e-061275982
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