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nsv7043112

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,299

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 22 studies. See in: genome view    
    Submitted genomic94,294,099-94,296,397Question Mark
    Overlapping variant regions from other studies: 123 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):94,759,655-94,761,953Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043112Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr194,294,09994,296,397
    nsv7043112RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr194,759,65594,761,953

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763347inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763347Submitted genomicNC_000001.11:g.942
    94099_94296397inv
    GRCh38 (hg38)NC_000001.11Chr194,294,09994,296,397
    nssv18763347RemappedPerfectNC_000001.10:g.947
    59655_94761953inv
    GRCh37.p13First PassNC_000001.10Chr194,759,65594,761,953

    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)
    nssv187633474e-061276268
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