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nsv7042253

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 20 studies. See in: genome view    
    Submitted genomic31,234,490-31,234,554Question Mark
    Overlapping variant regions from other studies: 96 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):31,234,597-31,234,661Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042253Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr531,234,49031,234,554
    nsv7042253RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr531,234,59731,234,661

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775764inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775764Submitted genomicNC_000005.10:g.312
    34490_31234554inv
    GRCh38 (hg38)NC_000005.10Chr531,234,49031,234,554
    nssv18775764RemappedPerfectNC_000005.9:g.3123
    4597_31234661inv
    GRCh37.p13First PassNC_000005.9Chr531,234,59731,234,661

    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)
    nssv187757644e-061276266
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