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nsv6804560

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:273,272

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 615 SVs from 63 studies. See in: genome view    
    Submitted genomic109,439,129-109,712,400Question Mark
    Overlapping variant regions from other studies: 615 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):109,760,332-110,033,603Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6804560Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6109,439,129109,712,400
    nsv6804560RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6109,760,332110,033,603

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18521060deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18521060Submitted genomicNC_000006.12:g.109
    439129_109712400de
    l
    GRCh38 (hg38)NC_000006.12Chr6109,439,129109,712,400
    nssv18521060RemappedPerfectNC_000006.11:g.109
    760332_110033603de
    l
    GRCh37.p13First PassNC_000006.11Chr6109,760,332110,033,603

    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)
    nssv185210601.1e-053275884
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