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nsv7075920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:119

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 19 studies. See in: genome view    
    Submitted genomic50,617,222-50,617,340Question Mark
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):52,376,982-52,377,100Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,617,22250,617,340
    nsv7075920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1052,376,98252,377,100

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731604inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731604Submitted genomicNC_000010.11:g.506
    17222_50617340inv
    GRCh38 (hg38)NC_000010.11Chr1050,617,22250,617,340
    nssv18731604RemappedPerfectNC_000010.10:g.523
    76982_52377100inv
    GRCh37.p13First PassNC_000010.10Chr1052,376,98252,377,100

    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)
    nssv187316047e-062276170
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