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nsv6993011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 156 SVs from 29 studies. See in: genome view    
    Submitted genomic58,902,101-58,914,300Question Mark
    Overlapping variant regions from other studies: 155 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):56,979,462-56,991,661Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1758,902,10158,914,300
    nsv6993011RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1756,979,46256,991,661

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413166deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413166Submitted genomicNC_000017.11:g.589
    02101_58914300del
    GRCh38 (hg38)NC_000017.11Chr1758,902,10158,914,300
    nssv18413166RemappedPerfectNC_000017.10:g.569
    79462_56991661del
    GRCh37.p13First PassNC_000017.10Chr1756,979,46256,991,661

    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)
    nssv18413166<0.00153252336
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