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nsv6863376

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:276,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 682 SVs from 63 studies. See in: genome view    
    Submitted genomic13,259,101-13,535,900Question Mark
    Overlapping variant regions from other studies: 687 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):13,259,100-13,535,899Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6863376Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr913,259,10113,535,900
    nsv6863376RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr913,259,10013,535,899

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736213duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736213Submitted genomicNC_000009.12:g.132
    59101_13535900dup
    GRCh38 (hg38)NC_000009.12Chr913,259,10113,535,900
    nssv18736213RemappedPerfectNC_000009.11:g.132
    59100_13535899dup
    GRCh37.p13First PassNC_000009.11Chr913,259,10013,535,899

    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)
    nssv187362134e-061275516
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