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nsv6976102

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,808

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 77 SVs from 20 studies. See in: genome view    
    Submitted genomic93,916,065-93,921,872Question Mark
    Overlapping variant regions from other studies: 79 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):94,382,411-94,388,218Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6976102Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1493,916,06593,921,872
    nsv6976102RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000014.8Chr1494,382,41194,388,218

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391955deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391955Submitted genomicNC_000014.9:g.9391
    6065_93921872del
    GRCh38 (hg38)NC_000014.9Chr1493,916,06593,921,872
    nssv18391955RemappedPerfectNC_000014.8:g.9438
    2411_94388218del
    GRCh37.p13Second PassNC_000014.8Chr1494,382,41194,388,218

    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)
    nssv183919551.4e-054275826
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