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nsv7044822

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 18 studies. See in: genome view    
    Submitted genomic109,398,820-109,398,856Question Mark
    Overlapping variant regions from other studies: 103 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):109,720,023-109,720,059Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044822Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6109,398,820109,398,856
    nsv7044822RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6109,720,023109,720,059

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776608inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776608Submitted genomicNC_000006.12:g.109
    398820_109398856in
    v
    GRCh38 (hg38)NC_000006.12Chr6109,398,820109,398,856
    nssv18776608RemappedPerfectNC_000006.11:g.109
    720023_109720059in
    v
    GRCh37.p13First PassNC_000006.11Chr6109,720,023109,720,059

    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)
    nssv18776608<0.00162274304
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