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nsv7001828

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:345,932

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 847 SVs from 67 studies. See in: genome view    
    Submitted genomic51,768,552-52,114,483Question Mark
    Overlapping variant regions from other studies: 847 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):52,271,805-52,617,736Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7001828Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1951,768,55252,114,483
    nsv7001828RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1952,271,80552,617,736

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638761duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638761Submitted genomicNC_000019.10:g.517
    68552_52114483dup
    GRCh38 (hg38)NC_000019.10Chr1951,768,55252,114,483
    nssv18638761RemappedPerfectNC_000019.9:g.5227
    1805_52617736dup
    GRCh37.p13First PassNC_000019.9Chr1952,271,80552,617,736

    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)
    nssv18638761<0.001128275238
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