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nsv6793869

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,181

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 26 studies. See in: genome view    
    Submitted genomic29,431,468-29,440,648Question Mark
    Overlapping variant regions from other studies: 104 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):29,399,245-29,408,425Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793869Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr629,431,46829,440,648
    nsv6793869RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr629,399,24529,408,425

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18714891duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18714891Submitted genomicNC_000006.12:g.294
    31468_29440648dup
    GRCh38 (hg38)NC_000006.12Chr629,431,46829,440,648
    nssv18714891RemappedPerfectNC_000006.11:g.293
    99245_29408425dup
    GRCh37.p13First PassNC_000006.11Chr629,399,24529,408,425

    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)
    nssv187148914e-061275558
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