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nsv6806891

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,509

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 33 studies. See in: genome view    
    Submitted genomic151,339,662-151,346,170Question Mark
    Overlapping variant regions from other studies: 140 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):151,660,797-151,667,305Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6806891Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6151,339,662151,346,170
    nsv6806891RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6151,660,797151,667,305

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18522800deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18522800Submitted genomicNC_000006.12:g.151
    339662_151346170de
    l
    GRCh38 (hg38)NC_000006.12Chr6151,339,662151,346,170
    nssv18522800RemappedPerfectNC_000006.11:g.151
    660797_151667305de
    l
    GRCh37.p13First PassNC_000006.11Chr6151,660,797151,667,305

    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)
    nssv185228004e-061275894
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