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nsv7077319

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:212,717

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1409 SVs from 79 studies. See in: genome view    
    Submitted genomic53,687,280-53,899,996Question Mark
    Overlapping variant regions from other studies: 1409 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):54,190,534-54,403,250Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077319Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,687,28053,899,996
    nsv7077319RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,190,53454,403,250

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760695inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760695Submitted genomicNC_000019.10:g.536
    87280_53899996inv
    GRCh38 (hg38)NC_000019.10Chr1953,687,28053,899,996
    nssv18760695RemappedPerfectNC_000019.9:g.5419
    0534_54403250inv
    GRCh37.p13First PassNC_000019.9Chr1954,190,53454,403,250

    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)
    nssv187606954e-061276268
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