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nsv6952768

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,786

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 206 SVs from 44 studies. See in: genome view    
    Submitted genomic20,684,552-20,730,337Question Mark
    Overlapping variant regions from other studies: 206 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):21,152,711-21,198,496Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6952768Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1420,684,55220,730,337
    nsv6952768RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1421,152,71121,198,496

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611029duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611029Submitted genomicNC_000014.9:g.2068
    4552_20730337dup
    GRCh38 (hg38)NC_000014.9Chr1420,684,55220,730,337
    nssv18611029RemappedPerfectNC_000014.8:g.2115
    2711_21198496dup
    GRCh37.p13First PassNC_000014.8Chr1421,152,71121,198,496

    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)
    nssv186110294e-061275378
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