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nsv7061841

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,867

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 21 studies. See in: genome view    
    Submitted genomic88,103,262-88,110,128Question Mark
    Overlapping variant regions from other studies: 122 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):88,646,493-88,653,359Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061841Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1588,103,26288,110,128
    nsv7061841RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1588,646,49388,653,359

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756082inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756082Submitted genomicNC_000015.10:g.881
    03262_88110128inv
    GRCh38 (hg38)NC_000015.10Chr1588,103,26288,110,128
    nssv18756082RemappedPerfectNC_000015.9:g.8864
    6493_88653359inv
    GRCh37.p13First PassNC_000015.9Chr1588,646,49388,653,359

    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)
    nssv187560821.1e-053275030
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