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nsv7070636

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,549

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 30 studies. See in: genome view    
    Submitted genomic42,241,109-42,256,657Question Mark
    Overlapping variant regions from other studies: 173 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):42,098,627-42,114,175Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070636Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr842,241,10942,256,657
    nsv7070636RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr842,098,62742,114,175

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782407inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782407Submitted genomicNC_000008.11:g.422
    41109_42256657inv
    GRCh38 (hg38)NC_000008.11Chr842,241,10942,256,657
    nssv18782407RemappedPerfectNC_000008.10:g.420
    98627_42114175inv
    GRCh37.p13First PassNC_000008.10Chr842,098,62742,114,175

    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)
    nssv187824074e-061276268
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