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nsv6870540

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,816

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view    
    Submitted genomic92,668,035-92,671,850Question Mark
    Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):95,430,317-95,434,132Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6870540Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr992,668,03592,671,850
    nsv6870540RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr995,430,31795,434,132

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18585294deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18585294Submitted genomicNC_000009.12:g.926
    68035_92671850del
    GRCh38 (hg38)NC_000009.12Chr992,668,03592,671,850
    nssv18585294RemappedPerfectNC_000009.11:g.954
    30317_95434132del
    GRCh37.p13First PassNC_000009.11Chr995,430,31795,434,132

    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)
    nssv185852947e-062276046
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