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nsv6708315

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 21 studies. See in: genome view    
    Submitted genomic122,853,374-122,853,443Question Mark
    Overlapping variant regions from other studies: 108 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):122,572,221-122,572,290Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6708315Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3122,853,374122,853,443
    nsv6708315RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3122,572,221122,572,290

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18471691deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18471691Submitted genomicNC_000003.12:g.122
    853374_122853443de
    l
    GRCh38 (hg38)NC_000003.12Chr3122,853,374122,853,443
    nssv18471691RemappedPerfectNC_000003.11:g.122
    572221_122572290de
    l
    GRCh37.p13First PassNC_000003.11Chr3122,572,221122,572,290

    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)
    nssv18471691<0.00138257856
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