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nsv6859584

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127,560

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 632 SVs from 51 studies. See in: genome view    
    Submitted genomic2,533,956-2,661,515Question Mark
    Overlapping variant regions from other studies: 634 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):2,533,956-2,661,515Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6859584Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr92,533,9562,661,515
    nsv6859584RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr92,533,9562,661,515

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18567492deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18567492Submitted genomicNC_000009.12:g.253
    3956_2661515del
    GRCh38 (hg38)NC_000009.12Chr92,533,9562,661,515
    nssv18567492RemappedPerfectNC_000009.11:g.253
    3956_2661515del
    GRCh37.p13First PassNC_000009.11Chr92,533,9562,661,515

    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)
    nssv185674924e-061276252
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