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nsv7062571

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
    Submitted genomic97,388,596-97,388,696Question Mark
    Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):99,148,353-99,148,453Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062571Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1097,388,59697,388,696
    nsv7062571RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1099,148,35399,148,453

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18733854inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18733854Submitted genomicNC_000010.11:g.973
    88596_97388696inv
    GRCh38 (hg38)NC_000010.11Chr1097,388,59697,388,696
    nssv18733854RemappedPerfectNC_000010.10:g.991
    48353_99148453inv
    GRCh37.p13First PassNC_000010.10Chr1099,148,35399,148,453

    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)
    nssv187338544e-061276268
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