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nsv7042498

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:846,973

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4327 SVs from 97 studies. See in: genome view    
    Submitted genomic246,214,057-247,061,029Question Mark
    Overlapping variant regions from other studies: 4330 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):246,377,359-247,224,331Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042498Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1246,214,057247,061,029
    nsv7042498RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1246,377,359247,224,331

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759482inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759482Submitted genomicNC_000001.11:g.246
    214057_247061029in
    v
    GRCh38 (hg38)NC_000001.11Chr1246,214,057247,061,029
    nssv18759482RemappedPerfectNC_000001.10:g.246
    377359_247224331in
    v
    GRCh37.p13First PassNC_000001.10Chr1246,377,359247,224,331

    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)
    nssv187594824e-061276268
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