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nsv6924593

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:467,135

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1620 SVs from 84 studies. See in: genome view    
    Submitted genomic19,243,454-19,710,588Question Mark
    Overlapping variant regions from other studies: 1620 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):19,817,594-20,284,728Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6924593Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1319,243,45419,710,588
    nsv6924593RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1319,817,59420,284,728

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18375985deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18375985Submitted genomicNC_000013.11:g.192
    43454_19710588del
    GRCh38 (hg38)NC_000013.11Chr1319,243,45419,710,588
    nssv18375985RemappedPerfectNC_000013.10:g.198
    17594_20284728del
    GRCh37.p13First PassNC_000013.10Chr1319,817,59420,284,728

    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)
    nssv183759851.1e-053276140
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