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nsv7058395

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,375

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 42 studies. See in: genome view    
    Submitted genomic37,249,810-37,253,184Question Mark
    Overlapping variant regions from other studies: 158 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):37,740,712-37,744,086Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058395Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1937,249,81037,253,184
    nsv7058395RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,740,71237,744,086

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758604inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758604Submitted genomicNC_000019.10:g.372
    49810_37253184inv
    GRCh38 (hg38)NC_000019.10Chr1937,249,81037,253,184
    nssv18758604RemappedPerfectNC_000019.9:g.3774
    0712_37744086inv
    GRCh37.p13First PassNC_000019.9Chr1937,740,71237,744,086

    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)
    nssv187586044e-061276268
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