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nsv7074310

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,778,670

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 18940 SVs from 126 studies. See in: genome view    
    Submitted genomic22,076,285-27,854,954Question Mark
    Overlapping variant regions from other studies: 19066 SVs from 126 studies. See in: genome view    
    Remapped(Score: Good):22,544,546-28,324,160Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074310Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1422,076,28527,854,954
    nsv7074310RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1422,544,54628,324,160

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754494inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754494Submitted genomicNC_000014.9:g.2207
    6285_27854954inv
    GRCh38 (hg38)NC_000014.9Chr1422,076,28527,854,954
    nssv18754494RemappedGoodNC_000014.8:g.2254
    4546_28324160inv
    GRCh37.p13First PassNC_000014.8Chr1422,544,54628,324,160

    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)
    nssv187544944e-061276268
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