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nsv6981121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:135,451

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 562 SVs from 55 studies. See in: genome view    
    Submitted genomic59,088,452-59,223,902Question Mark
    Overlapping variant regions from other studies: 561 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):57,165,813-57,301,263Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6981121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1759,088,45259,223,902
    nsv6981121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1757,165,81357,301,263

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413187deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413187Submitted genomicNC_000017.11:g.590
    88452_59223902del
    GRCh38 (hg38)NC_000017.11Chr1759,088,45259,223,902
    nssv18413187RemappedPerfectNC_000017.10:g.571
    65813_57301263del
    GRCh37.p13First PassNC_000017.10Chr1757,165,81357,301,263

    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)
    nssv184131874e-061276228
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