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nsv6856844

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:286,894

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 696 SVs from 64 studies. See in: genome view    
    Submitted genomic58,031,629-58,318,522Question Mark
    Overlapping variant regions from other studies: 696 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):58,944,188-59,231,081Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6856844Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr858,031,62958,318,522
    nsv6856844RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr858,944,18859,231,081

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18740584duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18740584Submitted genomicNC_000008.11:g.580
    31629_58318522dup
    GRCh38 (hg38)NC_000008.11Chr858,031,62958,318,522
    nssv18740584RemappedPerfectNC_000008.10:g.589
    44188_59231081dup
    GRCh37.p13First PassNC_000008.10Chr858,944,18859,231,081

    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)
    nssv187405844e-061275552
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