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nsv7058821

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 22 studies. See in: genome view    
    Submitted genomic56,315,730-56,315,748Question Mark
    Overlapping variant regions from other studies: 106 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):56,827,099-56,827,117Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058821Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1956,315,73056,315,748
    nsv7058821RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,827,09956,827,117

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761366inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761366Submitted genomicNC_000019.10:g.563
    15730_56315748inv
    GRCh38 (hg38)NC_000019.10Chr1956,315,73056,315,748
    nssv18761366RemappedPerfectNC_000019.9:g.5682
    7099_56827117inv
    GRCh37.p13First PassNC_000019.9Chr1956,827,09956,827,117

    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)
    nssv18761366<0.00168274798
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