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nsv6987795

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 186 SVs from 41 studies. See in: genome view    
    Submitted genomic28,051,901-28,106,200Question Mark
    Overlapping variant regions from other studies: 186 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):28,063,222-28,117,521Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6987795Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1628,051,90128,106,200
    nsv6987795RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1628,063,22228,117,521

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18622236duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18622236Submitted genomicNC_000016.10:g.280
    51901_28106200dup
    GRCh38 (hg38)NC_000016.10Chr1628,051,90128,106,200
    nssv18622236RemappedPerfectNC_000016.9:g.2806
    3222_28117521dup
    GRCh37.p13First PassNC_000016.9Chr1628,063,22228,117,521

    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)
    nssv186222364e-061275648
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