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nsv6720064

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:563,605

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2915 SVs from 96 studies. See in: genome view    
    Submitted genomic197,394,307-197,957,911Question Mark
    Overlapping variant regions from other studies: 2915 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):197,121,178-197,684,782Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6720064Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3197,394,307197,957,911
    nsv6720064RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3197,121,178197,684,782

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18675150duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18675150Submitted genomicNC_000003.12:g.197
    394307_197957911du
    p
    GRCh38 (hg38)NC_000003.12Chr3197,394,307197,957,911
    nssv18675150RemappedPerfectNC_000003.11:g.197
    121178_197684782du
    p
    GRCh37.p13First PassNC_000003.11Chr3197,121,178197,684,782

    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)
    nssv186751504e-061275768
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