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nsv6977654

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:135,882

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 539 SVs from 59 studies. See in: genome view    
    Submitted genomic1,592,232-1,728,113Question Mark
    Overlapping variant regions from other studies: 539 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):1,642,233-1,778,114Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977654Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,592,2321,728,113
    nsv6977654RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,642,2331,778,114

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18399287deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18399287Submitted genomicNC_000016.10:g.159
    2232_1728113del
    GRCh38 (hg38)NC_000016.10Chr161,592,2321,728,113
    nssv18399287RemappedPerfectNC_000016.9:g.1642
    233_1778114del
    GRCh37.p13First PassNC_000016.9Chr161,642,2331,778,114

    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)
    nssv183992874e-061276222
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