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nsv7064983

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 22 studies. See in: genome view    
    Submitted genomic69,940,608-69,940,638Question Mark
    Overlapping variant regions from other studies: 190 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):70,514,740-70,514,770Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064983Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1369,940,60869,940,638
    nsv7064983RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1370,514,74070,514,770

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753150inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753150Submitted genomicNC_000013.11:g.699
    40608_69940638inv
    GRCh38 (hg38)NC_000013.11Chr1369,940,60869,940,638
    nssv18753150RemappedPerfectNC_000013.10:g.705
    14740_70514770inv
    GRCh37.p13First PassNC_000013.10Chr1370,514,74070,514,770

    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)
    nssv187531504e-061276232
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