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nsv6848311

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 22 studies. See in: genome view    
    Submitted genomic67,472,371-67,472,418Question Mark
    Overlapping variant regions from other studies: 122 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):68,384,606-68,384,653Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6848311Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr867,472,37167,472,418
    nsv6848311RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr868,384,60668,384,653

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18555916deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18555916Submitted genomicNC_000008.11:g.674
    72371_67472418del
    GRCh38 (hg38)NC_000008.11Chr867,472,37167,472,418
    nssv18555916RemappedPerfectNC_000008.10:g.683
    84606_68384653del
    GRCh37.p13First PassNC_000008.10Chr868,384,60668,384,653

    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)
    nssv185559160.0234294189002
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