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nsv6577032

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:516

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
    Submitted genomic66,990,138-66,990,653Question Mark
    Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):67,024,041-67,024,556Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6577032Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1666,990,13866,990,653
    nsv6577032RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1667,024,04167,024,556

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18243590inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18243590Submitted genomicNC_000016.10:g.669
    90138_66990653inv
    GRCh38 (hg38)NC_000016.10Chr1666,990,13866,990,653
    nssv18243590RemappedPerfectNC_000016.9:g.6702
    4041_67024556inv
    GRCh37.p13First PassNC_000016.9Chr1667,024,04167,024,556

    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)
    nssv18243590<0.001135590
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