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nsv7064529

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:909,265

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3333 SVs from 111 studies. See in: genome view    
    Submitted genomic30,725,264-31,634,528Question Mark
    Overlapping variant regions from other studies: 3333 SVs from 111 studies. See in: genome view    
    Remapped(Score: Perfect):31,017,467-31,926,731Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064529Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1530,725,26431,634,528
    nsv7064529RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1531,017,46731,926,731

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755994inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755994Submitted genomicNC_000015.10:g.307
    25264_31634528inv
    GRCh38 (hg38)NC_000015.10Chr1530,725,26431,634,528
    nssv18755994RemappedPerfectNC_000015.9:g.3101
    7467_31926731inv
    GRCh37.p13First PassNC_000015.9Chr1531,017,46731,926,731

    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)
    nssv187559947e-062274768
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