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nsv7060098

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,225

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 25 studies. See in: genome view    
    Submitted genomic39,204,317-39,212,541Question Mark
    Overlapping variant regions from other studies: 155 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):39,061,836-39,070,060Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060098Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr839,204,31739,212,541
    nsv7060098RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr839,061,83639,070,060

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781583inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781583Submitted genomicNC_000008.11:g.392
    04317_39212541inv
    GRCh38 (hg38)NC_000008.11Chr839,204,31739,212,541
    nssv18781583RemappedPerfectNC_000008.10:g.390
    61836_39070060inv
    GRCh37.p13First PassNC_000008.10Chr839,061,83639,070,060

    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)
    nssv187815834e-061276268
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