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nsv7005575

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,620

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 267 SVs from 46 studies. See in: genome view    
    Submitted genomic50,494,124-50,538,743Question Mark
    Overlapping variant regions from other studies: 267 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):50,997,381-51,042,000Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7005575Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1950,494,12450,538,743
    nsv7005575RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1950,997,38151,042,000

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638694duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638694Submitted genomicNC_000019.10:g.504
    94124_50538743dup
    GRCh38 (hg38)NC_000019.10Chr1950,494,12450,538,743
    nssv18638694RemappedPerfectNC_000019.9:g.5099
    7381_51042000dup
    GRCh37.p13First PassNC_000019.9Chr1950,997,38151,042,000

    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)
    nssv186386944e-061255604
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