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nsv6815694

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:411,282

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1061 SVs from 65 studies. See in: genome view    
    Submitted genomic106,063,529-106,474,810Question Mark
    Overlapping variant regions from other studies: 1061 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):106,511,404-106,922,685Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6815694Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6106,063,529106,474,810
    nsv6815694RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6106,511,404106,922,685

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18708823duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18708823Submitted genomicNC_000006.12:g.106
    063529_106474810du
    p
    GRCh38 (hg38)NC_000006.12Chr6106,063,529106,474,810
    nssv18708823RemappedPerfectNC_000006.11:g.106
    511404_106922685du
    p
    GRCh37.p13First PassNC_000006.11Chr6106,511,404106,922,685

    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)
    nssv187088234e-061275162
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