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nsv7058956

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,510,746

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15860 SVs from 130 studies. See in: genome view    
    Submitted genomic8,224,000-12,734,745Question Mark
    Overlapping variant regions from other studies: 15860 SVs from 130 studies. See in: genome view    
    Remapped(Score: Perfect):8,081,522-12,592,254Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058956Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr88,224,00012,734,745
    nsv7058956RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr88,081,52212,592,254

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785394inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785394Submitted genomicNC_000008.11:g.822
    4000_12734745inv
    GRCh38 (hg38)NC_000008.11Chr88,224,00012,734,745
    nssv18785394RemappedPerfectNC_000008.10:g.808
    1522_12592254inv
    GRCh37.p13First PassNC_000008.10Chr88,081,52212,592,254

    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)
    nssv187853947e-062275084
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