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nsv7077344

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,396

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 25 studies. See in: genome view    
    Submitted genomic22,777,138-22,788,533Question Mark
    Overlapping variant regions from other studies: 98 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):22,798,684-22,810,079Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077344Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1122,777,13822,788,533
    nsv7077344RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1122,798,68422,810,079

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739050inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739050Submitted genomicNC_000011.10:g.227
    77138_22788533inv
    GRCh38 (hg38)NC_000011.10Chr1122,777,13822,788,533
    nssv18739050RemappedPerfectNC_000011.9:g.2279
    8684_22810079inv
    GRCh37.p13First PassNC_000011.9Chr1122,798,68422,810,079

    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)
    nssv187390501.8e-055275146
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