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nsv7065496

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,227,643

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 32779 SVs from 143 studies. See in: genome view    
    Submitted genomic20,672,644-28,900,286Question Mark
    Overlapping variant regions from other studies: 32602 SVs from 143 studies. See in: genome view    
    Remapped(Score: Good):20,877,973-29,145,432Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065496Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1520,672,64428,900,286
    nsv7065496RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1520,877,97329,145,432

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755903inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755903Submitted genomicNC_000015.10:g.206
    72644_28900286inv
    GRCh38 (hg38)NC_000015.10Chr1520,672,64428,900,286
    nssv18755903RemappedGoodNC_000015.9:g.2087
    7973_29145432inv
    GRCh37.p13First PassNC_000015.9Chr1520,877,97329,145,432

    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)
    nssv187559034e-061276268
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