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nsv7019621

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,443

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 250 SVs from 29 studies. See in: genome view    
    Submitted genomic68,663,808-68,678,250Question Mark
    Overlapping variant regions from other studies: 250 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):67,883,650-67,898,092Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7019621Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX68,663,80868,678,250
    nsv7019621RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX67,883,65067,898,092

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767124inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767124Submitted genomicNC_000023.11:g.686
    63808_68678250inv
    GRCh38 (hg38)NC_000023.11ChrX68,663,80868,678,250
    nssv18767124RemappedPerfectNC_000023.10:g.678
    83650_67898092inv
    GRCh37.p13First PassNC_000023.10ChrX67,883,65067,898,092

    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)
    nssv187671245e-061200000
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