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nsv6598038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,298,167

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 12271 SVs from 110 studies. See in: genome view    
    Submitted genomic45,719,988-49,018,154Question Mark
    Overlapping variant regions from other studies: 12272 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):46,223,246-49,521,411Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6598038Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1945,719,98849,018,154
    nsv6598038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1946,223,24649,521,411

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18245655inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18245655Submitted genomicNC_000019.10:g.457
    19988_49018154inv
    GRCh38 (hg38)NC_000019.10Chr1945,719,98849,018,154
    nssv18245655RemappedPerfectNC_000019.9:g.4622
    3246_49521411inv
    GRCh37.p13First PassNC_000019.9Chr1946,223,24649,521,411

    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)
    nssv18245655<0.001339304
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