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nsv7077791

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,681,670

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4552 SVs from 106 studies. See in: genome view    
    Submitted genomic117,677,720-119,359,389Question Mark
    Overlapping variant regions from other studies: 4552 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):118,689,959-120,371,629Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077791Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8117,677,720119,359,389
    nsv7077791RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8118,689,959120,371,629

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783754inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783754Submitted genomicNC_000008.11:g.117
    677720_119359389in
    v
    GRCh38 (hg38)NC_000008.11Chr8117,677,720119,359,389
    nssv18783754RemappedPerfectNC_000008.10:g.118
    689959_120371629in
    v
    GRCh37.p13First PassNC_000008.10Chr8118,689,959120,371,629

    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)
    nssv187837547e-062275090
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