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nsv7064380

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 17 studies. See in: genome view    
    Submitted genomic99,194,355-99,194,429Question Mark
    Overlapping variant regions from other studies: 151 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):99,846,609-99,846,683Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064380Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1399,194,35599,194,429
    nsv7064380RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1399,846,60999,846,683

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753321inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753321Submitted genomicNC_000013.11:g.991
    94355_99194429inv
    GRCh38 (hg38)NC_000013.11Chr1399,194,35599,194,429
    nssv18753321RemappedPerfectNC_000013.10:g.998
    46609_99846683inv
    GRCh37.p13First PassNC_000013.10Chr1399,846,60999,846,683

    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)
    nssv187533212.5e-057272928
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