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nsv6991374

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,216

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 243 SVs from 42 studies. See in: genome view    
    Submitted genomic84,318,164-84,331,379Question Mark
    Overlapping variant regions from other studies: 243 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):84,351,770-84,364,985Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6991374Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1684,318,16484,331,379
    nsv6991374RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1684,351,77084,364,985

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624081duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624081Submitted genomicNC_000016.10:g.843
    18164_84331379dup
    GRCh38 (hg38)NC_000016.10Chr1684,318,16484,331,379
    nssv18624081RemappedPerfectNC_000016.9:g.8435
    1770_84364985dup
    GRCh37.p13First PassNC_000016.9Chr1684,351,77084,364,985

    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)
    nssv186240814e-061275644
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