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nsv7060582

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62,726

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 389 SVs from 54 studies. See in: genome view    
    Submitted genomic16,886,000-16,948,725Question Mark
    Overlapping variant regions from other studies: 389 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):16,789,314-16,852,039Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060582Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1716,886,00016,948,725
    nsv7060582RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1716,789,31416,852,039

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756179inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756179Submitted genomicNC_000017.11:g.168
    86000_16948725inv
    GRCh38 (hg38)NC_000017.11Chr1716,886,00016,948,725
    nssv18756179RemappedPerfectNC_000017.10:g.167
    89314_16852039inv
    GRCh37.p13First PassNC_000017.10Chr1716,789,31416,852,039

    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)
    nssv187561794e-061276268
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