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nsv7070109

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:434,194

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1245 SVs from 77 studies. See in: genome view    
    Submitted genomic87,536,871-87,971,064Question Mark
    Overlapping variant regions from other studies: 1245 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):89,296,628-89,730,821Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1087,536,87187,971,064
    nsv7070109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1089,296,62889,730,821

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743123inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743123Submitted genomicNC_000010.11:g.875
    36871_87971064inv
    GRCh38 (hg38)NC_000010.11Chr1087,536,87187,971,064
    nssv18743123RemappedPerfectNC_000010.10:g.892
    96628_89730821inv
    GRCh37.p13First PassNC_000010.10Chr1089,296,62889,730,821

    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)
    nssv187431234e-061276268
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