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nsv6927016

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,308

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 279 SVs from 59 studies. See in: genome view    
    Submitted genomic22,866,551-22,878,858Question Mark
    Overlapping variant regions from other studies: 279 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):23,440,690-23,452,997Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6927016Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1322,866,55122,878,858
    nsv6927016RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1323,440,69023,452,997

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18376268deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18376268Submitted genomicNC_000013.11:g.228
    66551_22878858del
    GRCh38 (hg38)NC_000013.11Chr1322,866,55122,878,858
    nssv18376268RemappedPerfectNC_000013.10:g.234
    40690_23452997del
    GRCh37.p13First PassNC_000013.10Chr1323,440,69023,452,997

    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)
    nssv183762684e-061276032
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