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nsv7062223

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,946

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 35 studies. See in: genome view    
    Submitted genomic19,335,317-19,339,262Question Mark
    Overlapping variant regions from other studies: 141 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):19,624,246-19,628,191Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062223Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1019,335,31719,339,262
    nsv7062223RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1019,624,24619,628,191

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18733990inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18733990Submitted genomicNC_000010.11:g.193
    35317_19339262inv
    GRCh38 (hg38)NC_000010.11Chr1019,335,31719,339,262
    nssv18733990RemappedPerfectNC_000010.10:g.196
    24246_19628191inv
    GRCh37.p13First PassNC_000010.10Chr1019,624,24619,628,191

    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)
    nssv187339904e-061276268
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