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nsv7070672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:136

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 17 studies. See in: genome view    
    Submitted genomic33,676,015-33,676,150Question Mark
    Overlapping variant regions from other studies: 113 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):34,166,921-34,167,056Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1933,676,01533,676,150
    nsv7070672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1934,166,92134,167,056

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758556inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758556Submitted genomicNC_000019.10:g.336
    76015_33676150inv
    GRCh38 (hg38)NC_000019.10Chr1933,676,01533,676,150
    nssv18758556RemappedPerfectNC_000019.9:g.3416
    6921_34167056inv
    GRCh37.p13First PassNC_000019.9Chr1934,166,92134,167,056

    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)
    nssv18758556<0.00184270400
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