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nsv6811018

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 21 studies. See in: genome view    
    Submitted genomic137,160,301-137,163,400Question Mark
    Overlapping variant regions from other studies: 104 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):137,481,438-137,484,537Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6811018Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6137,160,301137,163,400
    nsv6811018RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6137,481,438137,484,537

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18522343deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18522343Submitted genomicNC_000006.12:g.137
    160301_137163400de
    l
    GRCh38 (hg38)NC_000006.12Chr6137,160,301137,163,400
    nssv18522343RemappedPerfectNC_000006.11:g.137
    481438_137484537de
    l
    GRCh37.p13First PassNC_000006.11Chr6137,481,438137,484,537

    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)
    nssv185223432.8e-058275444
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