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nsv6986015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:176,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 662 SVs from 64 studies. See in: genome view    
    Submitted genomic63,901,401-64,077,400Question Mark
    Overlapping variant regions from other studies: 662 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):61,978,761-62,154,760Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6986015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1763,901,40164,077,400
    nsv6986015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1761,978,76162,154,760

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628821duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628821Submitted genomicNC_000017.11:g.639
    01401_64077400dup
    GRCh38 (hg38)NC_000017.11Chr1763,901,40164,077,400
    nssv18628821RemappedPerfectNC_000017.10:g.619
    78761_62154760dup
    GRCh37.p13First PassNC_000017.10Chr1761,978,76162,154,760

    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)
    nssv186288214e-061269138
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