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nsv7031368

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,388

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 270 SVs from 19 studies. See in: genome view    
    Submitted genomic24,203,101-24,207,488Question Mark
    Overlapping variant regions from other studies: 271 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):24,221,218-24,225,605Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7031368Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX24,203,10124,207,488
    nsv7031368RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX24,221,21824,225,605

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18764330inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18764330Submitted genomicNC_000023.11:g.242
    03101_24207488inv
    GRCh38 (hg38)NC_000023.11ChrX24,203,10124,207,488
    nssv18764330RemappedPerfectNC_000023.10:g.242
    21218_24225605inv
    GRCh37.p13First PassNC_000023.10ChrX24,221,21824,225,605

    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)
    nssv187643305e-061200000
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