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nsv7061639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,653

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 32 studies. See in: genome view    
    Submitted genomic27,464,374-27,476,026Question Mark
    Overlapping variant regions from other studies: 196 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):27,464,372-27,476,024Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr927,464,37427,476,026
    nsv7061639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr927,464,37227,476,024

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784611inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784611Submitted genomicNC_000009.12:g.274
    64374_27476026inv
    GRCh38 (hg38)NC_000009.12Chr927,464,37427,476,026
    nssv18784611RemappedPerfectNC_000009.11:g.274
    64372_27476024inv
    GRCh37.p13First PassNC_000009.11Chr927,464,37227,476,024

    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)
    nssv187846114e-061276268
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