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nsv6981326

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,738

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 24 studies. See in: genome view    
    Submitted genomic49,018,130-49,020,867Question Mark
    Overlapping variant regions from other studies: 139 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):47,095,492-47,098,229Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6981326Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1749,018,13049,020,867
    nsv6981326RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1747,095,49247,098,229

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18411034deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18411034Submitted genomicNC_000017.11:g.490
    18130_49020867del
    GRCh38 (hg38)NC_000017.11Chr1749,018,13049,020,867
    nssv18411034RemappedPerfectNC_000017.10:g.470
    95492_47098229del
    GRCh37.p13First PassNC_000017.10Chr1747,095,49247,098,229

    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)
    nssv184110346.5e-0518269028
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