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nsv6985882

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:146,788

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 653 SVs from 66 studies. See in: genome view    
    Submitted genomic77,151,422-77,298,209Question Mark
    Overlapping variant regions from other studies: 653 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):77,185,319-77,332,106Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6985882Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1677,151,42277,298,209
    nsv6985882RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1677,185,31977,332,106

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18625304duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18625304Submitted genomicNC_000016.10:g.771
    51422_77298209dup
    GRCh38 (hg38)NC_000016.10Chr1677,151,42277,298,209
    nssv18625304RemappedPerfectNC_000016.9:g.7718
    5319_77332106dup
    GRCh37.p13First PassNC_000016.9Chr1677,185,31977,332,106

    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)
    nssv186253044e-061275374
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