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nsv6982129

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 32 studies. See in: genome view    
    Submitted genomic7,678,101-7,685,800Question Mark
    Overlapping variant regions from other studies: 181 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):7,581,419-7,589,118Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6982129Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr177,678,1017,685,800
    nsv6982129RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr177,581,4197,589,118

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631630duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631630Submitted genomicNC_000017.11:g.767
    8101_7685800dup
    GRCh38 (hg38)NC_000017.11Chr177,678,1017,685,800
    nssv18631630RemappedPerfectNC_000017.10:g.758
    1419_7589118dup
    GRCh37.p13First PassNC_000017.10Chr177,581,4197,589,118

    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)
    nssv186316305.5e-0515266694
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