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nsv7061393

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,270,539

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3119 SVs from 96 studies. See in: genome view    
    Submitted genomic125,582,588-126,853,126Question Mark
    Overlapping variant regions from other studies: 3119 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):127,271,157-128,541,695Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061393Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10125,582,588126,853,126
    nsv7061393RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10127,271,157128,541,695

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734310inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734310Submitted genomicNC_000010.11:g.125
    582588_126853126in
    v
    GRCh38 (hg38)NC_000010.11Chr10125,582,588126,853,126
    nssv18734310RemappedPerfectNC_000010.10:g.127
    271157_128541695in
    v
    GRCh37.p13First PassNC_000010.10Chr10127,271,157128,541,695

    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)
    nssv187343101.1e-053274996
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