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nsv6735396

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,824

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 81 SVs from 18 studies. See in: genome view    
    Submitted genomic46,946,997-46,948,820Question Mark
    Overlapping variant regions from other studies: 81 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):46,949,014-46,950,837Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6735396Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr446,946,99746,948,820
    nsv6735396RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr446,949,01446,950,837

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18690833duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18690833Submitted genomicNC_000004.12:g.469
    46997_46948820dup
    GRCh38 (hg38)NC_000004.12Chr446,946,99746,948,820
    nssv18690833RemappedPerfectNC_000004.11:g.469
    49014_46950837dup
    GRCh37.p13First PassNC_000004.11Chr446,949,01446,950,837

    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)
    nssv186908334e-061271400
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