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nsv6964107

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,911

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 20 studies. See in: genome view    
    Submitted genomic65,127,219-65,132,129Question Mark
    Overlapping variant regions from other studies: 98 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):65,419,557-65,424,467Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6964107Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1565,127,21965,132,129
    nsv6964107RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1565,419,55765,424,467

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18395699deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18395699Submitted genomicNC_000015.10:g.651
    27219_65132129del
    GRCh38 (hg38)NC_000015.10Chr1565,127,21965,132,129
    nssv18395699RemappedPerfectNC_000015.9:g.6541
    9557_65424467del
    GRCh37.p13First PassNC_000015.9Chr1565,419,55765,424,467

    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)
    nssv183956991.1e-053275636
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