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nsv6715346

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:121,087

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 382 SVs from 45 studies. See in: genome view    
    Submitted genomic113,491,847-113,612,933Question Mark
    Overlapping variant regions from other studies: 382 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):113,210,694-113,331,780Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6715346Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3113,491,847113,612,933
    nsv6715346RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3113,210,694113,331,780

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18471287deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18471287Submitted genomicNC_000003.12:g.113
    491847_113612933de
    l
    GRCh38 (hg38)NC_000003.12Chr3113,491,847113,612,933
    nssv18471287RemappedPerfectNC_000003.11:g.113
    210694_113331780de
    l
    GRCh37.p13First PassNC_000003.11Chr3113,210,694113,331,780

    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)
    nssv184712874e-061276256
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