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nsv7073489

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,939,221

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8375 SVs from 122 studies. See in: genome view    
    Submitted genomic48,372,840-50,312,060Question Mark
    Overlapping variant regions from other studies: 8348 SVs from 122 studies. See in: genome view    
    Remapped(Score: Good):48,394,392-50,271,231Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073489Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1148,372,84050,312,060
    nsv7073489RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1148,394,39250,271,231

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18744860inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18744860Submitted genomicNC_000011.10:g.483
    72840_50312060inv
    GRCh38 (hg38)NC_000011.10Chr1148,372,84050,312,060
    nssv18744860RemappedGoodNC_000011.9:g.4839
    4392_50271231inv
    GRCh37.p13First PassNC_000011.9Chr1148,394,39250,271,231

    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)
    nssv187448604e-061276266
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