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nsv6725178

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:746,152

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1572 SVs from 81 studies. See in: genome view    
    Submitted genomic158,267,158-159,013,309Question Mark
    Overlapping variant regions from other studies: 1572 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):157,984,947-158,731,098Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6725178Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3158,267,158159,013,309
    nsv6725178RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3157,984,947158,731,098

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18673686duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18673686Submitted genomicNC_000003.12:g.158
    267158_159013309du
    p
    GRCh38 (hg38)NC_000003.12Chr3158,267,158159,013,309
    nssv18673686RemappedPerfectNC_000003.11:g.157
    984947_158731098du
    p
    GRCh37.p13First PassNC_000003.11Chr3157,984,947158,731,098

    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)
    nssv186736864e-061275188
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