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nsv6989115

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109,321

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 447 SVs from 49 studies. See in: genome view    
    Submitted genomic7,900,907-8,010,227Question Mark
    Overlapping variant regions from other studies: 447 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):7,804,225-7,913,545Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6989115Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr177,900,9078,010,227
    nsv6989115RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr177,804,2257,913,545

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631753duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631753Submitted genomicNC_000017.11:g.790
    0907_8010227dup
    GRCh38 (hg38)NC_000017.11Chr177,900,9078,010,227
    nssv18631753RemappedPerfectNC_000017.10:g.780
    4225_7913545dup
    GRCh37.p13First PassNC_000017.10Chr177,804,2257,913,545

    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)
    nssv186317537e-062275204
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