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nsv6927865

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
    Submitted genomic53,397,963-53,402,062Question Mark
    Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):53,791,747-53,795,846Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6927865Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,397,96353,402,062
    nsv6927865RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,791,74753,795,846

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18361170deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18361170Submitted genomicNC_000012.12:g.533
    97963_53402062del
    GRCh38 (hg38)NC_000012.12Chr1253,397,96353,402,062
    nssv18361170RemappedPerfectNC_000012.11:g.537
    91747_53795846del
    GRCh37.p13First PassNC_000012.11Chr1253,791,74753,795,846

    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)
    nssv183611707e-061276232
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