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nsv6871104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,449

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 29 studies. See in: genome view    
    Submitted genomic89,450,916-89,457,364Question Mark
    Overlapping variant regions from other studies: 107 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):92,065,831-92,072,279Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6871104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr989,450,91689,457,364
    nsv6871104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr992,065,83192,072,279

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18590982deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18590982Submitted genomicNC_000009.12:g.894
    50916_89457364del
    GRCh38 (hg38)NC_000009.12Chr989,450,91689,457,364
    nssv18590982RemappedPerfectNC_000009.11:g.920
    65831_92072279del
    GRCh37.p13First PassNC_000009.11Chr992,065,83192,072,279

    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)
    nssv185909824e-061276262
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