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nsv7074407

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:588,467

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3347 SVs from 120 studies. See in: genome view    
    Submitted genomic7,895,385-8,483,851Question Mark
    Overlapping variant regions from other studies: 3347 SVs from 120 studies. See in: genome view    
    Remapped(Score: Perfect):8,047,981-8,636,447Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074407Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,895,3858,483,851
    nsv7074407RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr128,047,9818,636,447

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752463inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752463Submitted genomicNC_000012.12:g.789
    5385_8483851inv
    GRCh38 (hg38)NC_000012.12Chr127,895,3858,483,851
    nssv18752463RemappedPerfectNC_000012.11:g.804
    7981_8636447inv
    GRCh37.p13First PassNC_000012.11Chr128,047,9818,636,447

    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)
    nssv187524631.1e-053274002
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