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nsv6648304

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,893

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
    Submitted genomic28,591,780-28,593,672Question Mark
    Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):28,918,292-28,920,184Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6648304Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr128,591,78028,593,672
    nsv6648304RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr128,918,29228,920,184

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18389223deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18389223Submitted genomicNC_000001.11:g.285
    91780_28593672del
    GRCh38 (hg38)NC_000001.11Chr128,591,78028,593,672
    nssv18389223RemappedPerfectNC_000001.10:g.289
    18292_28920184del
    GRCh37.p13First PassNC_000001.10Chr128,918,29228,920,184

    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)
    nssv183892232.5e-057273086
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