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nsv7072115

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,876,854

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7351 SVs from 108 studies. See in: genome view    
    Submitted genomic12,276,809-15,153,662Question Mark
    Overlapping variant regions from other studies: 7357 SVs from 108 studies. See in: genome view    
    Remapped(Score: Perfect):12,276,809-15,153,660Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072115Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr912,276,80915,153,662
    nsv7072115RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr912,276,80915,153,660

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784337inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784337Submitted genomicNC_000009.12:g.122
    76809_15153662inv
    GRCh38 (hg38)NC_000009.12Chr912,276,80915,153,662
    nssv18784337RemappedPerfectNC_000009.11:g.122
    76809_15153660inv
    GRCh37.p13First PassNC_000009.11Chr912,276,80915,153,660

    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)
    nssv187843374e-061276268
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