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nsv7000416

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,429

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 196 SVs from 38 studies. See in: genome view    
    Submitted genomic17,240,841-17,259,269Question Mark
    Overlapping variant regions from other studies: 196 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):17,351,650-17,370,078Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7000416Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1917,240,84117,259,269
    nsv7000416RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1917,351,65017,370,078

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639312duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639312Submitted genomicNC_000019.10:g.172
    40841_17259269dup
    GRCh38 (hg38)NC_000019.10Chr1917,240,84117,259,269
    nssv18639312RemappedPerfectNC_000019.9:g.1735
    1650_17370078dup
    GRCh37.p13First PassNC_000019.9Chr1917,351,65017,370,078

    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)
    nssv186393124e-061276050
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