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nsv7062634

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,724

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 164 SVs from 34 studies. See in: genome view    
    Submitted genomic74,348,013-74,353,736Question Mark
    Overlapping variant regions from other studies: 164 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):74,640,354-74,646,077Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062634Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1574,348,01374,353,736
    nsv7062634RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1574,640,35474,646,077

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755065inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755065Submitted genomicNC_000015.10:g.743
    48013_74353736inv
    GRCh38 (hg38)NC_000015.10Chr1574,348,01374,353,736
    nssv18755065RemappedPerfectNC_000015.9:g.7464
    0354_74646077inv
    GRCh37.p13First PassNC_000015.9Chr1574,640,35474,646,077

    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)
    nssv187550654e-061276268
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