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nsv6986147

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:257

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 15 studies. See in: genome view    
    Submitted genomic68,428,365-68,428,621Question Mark
    Overlapping variant regions from other studies: 99 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):66,424,506-66,424,762Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6986147Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1768,428,36568,428,621
    nsv6986147RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1766,424,50666,424,762

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627689duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627689Submitted genomicNC_000017.11:g.684
    28365_68428621dup
    GRCh38 (hg38)NC_000017.11Chr1768,428,36568,428,621
    nssv18627689RemappedPerfectNC_000017.10:g.664
    24506_66424762dup
    GRCh37.p13First PassNC_000017.10Chr1766,424,50666,424,762

    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)
    nssv186276898e-062235520
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