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nsv6740177

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,254

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 27 studies. See in: genome view    
    Submitted genomic143,433,318-143,434,571Question Mark
    Overlapping variant regions from other studies: 131 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):144,354,471-144,355,724Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6740177Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4143,433,318143,434,571
    nsv6740177RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4144,354,471144,355,724

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18683933duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18683933Submitted genomicNC_000004.12:g.143
    433318_143434571du
    p
    GRCh38 (hg38)NC_000004.12Chr4143,433,318143,434,571
    nssv18683933RemappedPerfectNC_000004.11:g.144
    354471_144355724du
    p
    GRCh37.p13First PassNC_000004.11Chr4144,354,471144,355,724

    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)
    nssv186839334e-061267680
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