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nsv7058897

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 23 studies. See in: genome view    
    Submitted genomic142,345,706-142,345,832Question Mark
    Overlapping variant regions from other studies: 158 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):143,427,067-143,427,193Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058897Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8142,345,706142,345,832
    nsv7058897RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8143,427,067143,427,193

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783433inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783433Submitted genomicNC_000008.11:g.142
    345706_142345832in
    v
    GRCh38 (hg38)NC_000008.11Chr8142,345,706142,345,832
    nssv18783433RemappedPerfectNC_000008.10:g.143
    427067_143427193in
    v
    GRCh37.p13First PassNC_000008.10Chr8143,427,067143,427,193

    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)
    nssv187834334e-061276268
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