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nsv6979493

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:374

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 218 SVs from 38 studies. See in: genome view    
    Submitted genomic14,339,341-14,339,714Question Mark
    Overlapping variant regions from other studies: 218 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):14,242,658-14,243,031Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6979493Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1714,339,34114,339,714
    nsv6979493RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1714,242,65814,243,031

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626305duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626305Submitted genomicNC_000017.11:g.143
    39341_14339714dup
    GRCh38 (hg38)NC_000017.11Chr1714,339,34114,339,714
    nssv18626305RemappedPerfectNC_000017.10:g.142
    42658_14243031dup
    GRCh37.p13First PassNC_000017.10Chr1714,242,65814,243,031

    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)
    nssv186263054e-061239858
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