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nsv7070941

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,131

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 26 studies. See in: genome view    
    Submitted genomic90,998,357-90,999,487Question Mark
    Overlapping variant regions from other studies: 101 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):91,392,134-91,393,264Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070941Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1290,998,35790,999,487
    nsv7070941RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1291,392,13491,393,264

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753549inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753549Submitted genomicNC_000012.12:g.909
    98357_90999487inv
    GRCh38 (hg38)NC_000012.12Chr1290,998,35790,999,487
    nssv18753549RemappedPerfectNC_000012.11:g.913
    92134_91393264inv
    GRCh37.p13First PassNC_000012.11Chr1291,392,13491,393,264

    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)
    nssv187535494e-061276264
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