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nsv6575760

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:683,456

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2098 SVs from 101 studies. See in: genome view    
    Submitted genomic79,538,320-80,221,775Question Mark
    Overlapping variant regions from other studies: 2169 SVs from 105 studies. See in: genome view    
    Remapped(Score: Perfect):81,298,076-81,981,531Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6575760Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1079,538,32080,221,775
    nsv6575760RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1081,298,07681,981,531

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18231262inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18231262Submitted genomicNC_000010.11:g.795
    38320_80221775inv
    GRCh38 (hg38)NC_000010.11Chr1079,538,32080,221,775
    nssv18231262RemappedPerfectNC_000010.10:g.812
    98076_81981531inv
    GRCh37.p13First PassNC_000010.10Chr1081,298,07681,981,531

    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)
    nssv18231262<0.001139300
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