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nsv7077156

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:429,692

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1447 SVs from 80 studies. See in: genome view    
    Submitted genomic36,692,829-37,122,520Question Mark
    Overlapping variant regions from other studies: 1447 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):37,183,731-37,613,422Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077156Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,692,82937,122,520
    nsv7077156RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,183,73137,613,422

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758593inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758593Submitted genomicNC_000019.10:g.366
    92829_37122520inv
    GRCh38 (hg38)NC_000019.10Chr1936,692,82937,122,520
    nssv18758593RemappedPerfectNC_000019.9:g.3718
    3731_37613422inv
    GRCh37.p13First PassNC_000019.9Chr1937,183,73137,613,422

    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)
    nssv187585938.9e-0525274018
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