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nsv7052357

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,036

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 26 studies. See in: genome view    
    Submitted genomic165,071,350-165,072,385Question Mark
    Overlapping variant regions from other studies: 158 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):165,992,502-165,993,537Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052357Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4165,071,350165,072,385
    nsv7052357RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4165,992,502165,993,537

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773145inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773145Submitted genomicNC_000004.12:g.165
    071350_165072385in
    v
    GRCh38 (hg38)NC_000004.12Chr4165,071,350165,072,385
    nssv18773145RemappedPerfectNC_000004.11:g.165
    992502_165993537in
    v
    GRCh37.p13First PassNC_000004.11Chr4165,992,502165,993,537

    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)
    nssv18773145<0.00170267772
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