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nsv6565031

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,347,668

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 20236 SVs from 118 studies. See in: genome view    
    Submitted genomic22,900,235-30,247,902Question Mark
    Overlapping variant regions from other studies: 20241 SVs from 118 studies. See in: genome view    
    Remapped(Score: Perfect):22,757,748-30,105,418Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6565031Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr822,900,23530,247,902
    nsv6565031RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr822,757,74830,105,418

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18277486inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18277486Submitted genomicNC_000008.11:g.229
    00235_30247902inv
    GRCh38 (hg38)NC_000008.11Chr822,900,23530,247,902
    nssv18277486RemappedPerfectNC_000008.10:g.227
    57748_30105418inv
    GRCh37.p13First PassNC_000008.10Chr822,757,74830,105,418

    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)
    nssv18277486<0.001339218
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