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nsv6599769

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,156,862

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9059 SVs from 111 studies. See in: genome view    
    Submitted genomic21,518,661-23,675,522Question Mark
    Overlapping variant regions from other studies: 9059 SVs from 111 studies. See in: genome view    
    Remapped(Score: Perfect):21,701,463-23,858,324Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6599769Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1921,518,66123,675,522
    nsv6599769RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1921,701,46323,858,324

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18244888inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18244888Submitted genomicNC_000019.10:g.215
    18661_23675522inv
    GRCh38 (hg38)NC_000019.10Chr1921,518,66123,675,522
    nssv18244888RemappedPerfectNC_000019.9:g.2170
    1463_23858324inv
    GRCh37.p13First PassNC_000019.9Chr1921,701,46323,858,324

    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)
    nssv182448880.01429721332
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