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nsv7058036

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,464,996

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7408 SVs from 107 studies. See in: genome view    
    Submitted genomic94,195,543-97,660,538Question Mark
    Overlapping variant regions from other studies: 7409 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):93,531,248-96,996,242Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058036Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr594,195,54397,660,538
    nsv7058036RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr593,531,24896,996,242

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777012inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777012Submitted genomicNC_000005.10:g.941
    95543_97660538inv
    GRCh38 (hg38)NC_000005.10Chr594,195,54397,660,538
    nssv18777012RemappedPerfectNC_000005.9:g.9353
    1248_96996242inv
    GRCh37.p13First PassNC_000005.9Chr593,531,24896,996,242

    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)
    nssv187770124e-061276268
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