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nsv7047196

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,588

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 32 studies. See in: genome view    
    Submitted genomic21,636,961-21,643,548Question Mark
    Overlapping variant regions from other studies: 148 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):21,638,584-21,645,171Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047196Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr421,636,96121,643,548
    nsv7047196RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr421,638,58421,645,171

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773374inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773374Submitted genomicNC_000004.12:g.216
    36961_21643548inv
    GRCh38 (hg38)NC_000004.12Chr421,636,96121,643,548
    nssv18773374RemappedPerfectNC_000004.11:g.216
    38584_21645171inv
    GRCh37.p13First PassNC_000004.11Chr421,638,58421,645,171

    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)
    nssv187733744e-061276268
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