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nsv7072490

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:97,374

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 534 SVs from 57 studies. See in: genome view    
    Submitted genomic43,438,672-43,536,045Question Mark
    Overlapping variant regions from other studies: 534 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):43,942,824-44,040,197Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072490Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1943,438,67243,536,045
    nsv7072490RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1943,942,82444,040,197

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760774inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760774Submitted genomicNC_000019.10:g.434
    38672_43536045inv
    GRCh38 (hg38)NC_000019.10Chr1943,438,67243,536,045
    nssv18760774RemappedPerfectNC_000019.9:g.4394
    2824_44040197inv
    GRCh37.p13First PassNC_000019.9Chr1943,942,82444,040,197

    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)
    nssv187607747e-062275068
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