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nsv7056082

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,197

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 26 studies. See in: genome view    
    Submitted genomic34,111,345-34,120,541Question Mark
    Overlapping variant regions from other studies: 110 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):34,079,122-34,088,318Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056082Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr634,111,34534,120,541
    nsv7056082RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr634,079,12234,088,318

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778635inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778635Submitted genomicNC_000006.12:g.341
    11345_34120541inv
    GRCh38 (hg38)NC_000006.12Chr634,111,34534,120,541
    nssv18778635RemappedPerfectNC_000006.11:g.340
    79122_34088318inv
    GRCh37.p13First PassNC_000006.11Chr634,079,12234,088,318

    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)
    nssv187786357.9e-0522272990
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