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nsv6893070

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,649

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 150 SVs from 29 studies. See in: genome view    
    Submitted genomic124,441,373-124,453,021Question Mark
    Overlapping variant regions from other studies: 150 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):126,129,942-126,141,590Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6893070Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10124,441,373124,453,021
    nsv6893070RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10126,129,942126,141,590

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18576637duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18576637Submitted genomicNC_000010.11:g.124
    441373_124453021du
    p
    GRCh38 (hg38)NC_000010.11Chr10124,441,373124,453,021
    nssv18576637RemappedPerfectNC_000010.10:g.126
    129942_126141590du
    p
    GRCh37.p13First PassNC_000010.10Chr10126,129,942126,141,590

    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)
    nssv185766374e-061273918
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