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nsv7057600

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,112

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 30 studies. See in: genome view    
    Submitted genomic156,821,546-156,826,657Question Mark
    Overlapping variant regions from other studies: 145 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):157,742,698-157,747,809Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057600Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4156,821,546156,826,657
    nsv7057600RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4157,742,698157,747,809

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772984inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772984Submitted genomicNC_000004.12:g.156
    821546_156826657in
    v
    GRCh38 (hg38)NC_000004.12Chr4156,821,546156,826,657
    nssv18772984RemappedPerfectNC_000004.11:g.157
    742698_157747809in
    v
    GRCh37.p13First PassNC_000004.11Chr4157,742,698157,747,809

    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)
    nssv187729844e-061276268
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