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nsv7074300

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:372

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 30 studies. See in: genome view    
    Submitted genomic88,026,122-88,026,493Question Mark
    Overlapping variant regions from other studies: 114 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):87,759,290-87,759,661Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074300Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1188,026,12288,026,493
    nsv7074300RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1187,759,29087,759,661

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18742216inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18742216Submitted genomicNC_000011.10:g.880
    26122_88026493inv
    GRCh38 (hg38)NC_000011.10Chr1188,026,12288,026,493
    nssv18742216RemappedPerfectNC_000011.9:g.8775
    9290_87759661inv
    GRCh37.p13First PassNC_000011.9Chr1187,759,29087,759,661

    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)
    nssv18742216<0.001106264382
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