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nsv6591309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:486

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 185 SVs from 16 studies. See in: genome view    
    Submitted genomic130,384,553-130,385,038Question Mark
    Overlapping variant regions from other studies: 185 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):130,254,448-130,254,933Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6591309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11130,384,553130,385,038
    nsv6591309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11130,254,448130,254,933

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18221150inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18221150Submitted genomicNC_000011.10:g.130
    384553_130385038in
    v
    GRCh38 (hg38)NC_000011.10Chr11130,384,553130,385,038
    nssv18221150RemappedPerfectNC_000011.9:g.1302
    54448_130254933inv
    GRCh37.p13First PassNC_000011.9Chr11130,254,448130,254,933

    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)
    nssv18221150<0.001234430
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