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nsv6673153

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,483

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 24 studies. See in: genome view    
    Submitted genomic192,359,375-192,363,857Question Mark
    Overlapping variant regions from other studies: 141 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):192,328,505-192,332,987Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6673153Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1192,359,375192,363,857
    nsv6673153RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1192,328,505192,332,987

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18607014duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18607014Submitted genomicNC_000001.11:g.192
    359375_192363857du
    p
    GRCh38 (hg38)NC_000001.11Chr1192,359,375192,363,857
    nssv18607014RemappedPerfectNC_000001.10:g.192
    328505_192332987du
    p
    GRCh37.p13First PassNC_000001.10Chr1192,328,505192,332,987

    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)
    nssv186070144e-061274620
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