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nsv6976934

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,586

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 36 studies. See in: genome view    
    Submitted genomic55,493,339-55,530,924Question Mark
    Overlapping variant regions from other studies: 198 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):55,785,537-55,823,122Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6976934Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1555,493,33955,530,924
    nsv6976934RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1555,785,53755,823,122

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617322duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617322Submitted genomicNC_000015.10:g.554
    93339_55530924dup
    GRCh38 (hg38)NC_000015.10Chr1555,493,33955,530,924
    nssv18617322RemappedPerfectNC_000015.9:g.5578
    5537_55823122dup
    GRCh37.p13First PassNC_000015.9Chr1555,785,53755,823,122

    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)
    nssv186173221.1e-053275350
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