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nsv6974997

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,639

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 31 studies. See in: genome view    
    Submitted genomic59,514,309-59,528,947Question Mark
    Overlapping variant regions from other studies: 146 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):59,806,508-59,821,146Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6974997Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1559,514,30959,528,947
    nsv6974997RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,806,50859,821,146

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620286duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620286Submitted genomicNC_000015.10:g.595
    14309_59528947dup
    GRCh38 (hg38)NC_000015.10Chr1559,514,30959,528,947
    nssv18620286RemappedPerfectNC_000015.9:g.5980
    6508_59821146dup
    GRCh37.p13First PassNC_000015.9Chr1559,806,50859,821,146

    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)
    nssv186202864e-061275636
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