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nsv6681330

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,357

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 149 SVs from 33 studies. See in: genome view    
    Submitted genomic99,303,946-99,305,302Question Mark
    Overlapping variant regions from other studies: 149 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):99,920,409-99,921,765Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6681330Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr299,303,94699,305,302
    nsv6681330RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr299,920,40999,921,765

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18470866deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18470866Submitted genomicNC_000002.12:g.993
    03946_99305302del
    GRCh38 (hg38)NC_000002.12Chr299,303,94699,305,302
    nssv18470866RemappedPerfectNC_000002.11:g.999
    20409_99921765del
    GRCh37.p13First PassNC_000002.11Chr299,920,40999,921,765

    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)
    nssv184708663.6e-0510274574
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