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nsv6787298

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:370

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 73 SVs from 12 studies. See in: genome view    
    Submitted genomic160,349,066-160,349,435Question Mark
    Overlapping variant regions from other studies: 73 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):159,776,073-159,776,442Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6787298Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5160,349,066160,349,435
    nsv6787298RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5159,776,073159,776,442

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18697772duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18697772Submitted genomicNC_000005.10:g.160
    349066_160349435du
    p
    GRCh38 (hg38)NC_000005.10Chr5160,349,066160,349,435
    nssv18697772RemappedPerfectNC_000005.9:g.1597
    76073_159776442dup
    GRCh37.p13First PassNC_000005.9Chr5159,776,073159,776,442

    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)
    nssv186977724e-061240608
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