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nsv7052690

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:192,665

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 450 SVs from 55 studies. See in: genome view    
    Submitted genomic42,600,188-42,792,852Question Mark
    Overlapping variant regions from other studies: 450 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):42,639,787-42,832,451Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052690Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr742,600,18842,792,852
    nsv7052690RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr742,639,78742,832,451

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782682inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782682Submitted genomicNC_000007.14:g.426
    00188_42792852inv
    GRCh38 (hg38)NC_000007.14Chr742,600,18842,792,852
    nssv18782682RemappedPerfectNC_000007.13:g.426
    39787_42832451inv
    GRCh37.p13First PassNC_000007.13Chr742,639,78742,832,451

    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)
    nssv187826824.3e-0512275018
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