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nsv6860528

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:278,210

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1063 SVs from 69 studies. See in: genome view    
    Submitted genomic2,469,791-2,748,000Question Mark
    Overlapping variant regions from other studies: 1065 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):2,469,791-2,748,000Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6860528Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr92,469,7912,748,000
    nsv6860528RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr92,469,7912,748,000

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18568107deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18568107Submitted genomicNC_000009.12:g.246
    9791_2748000del
    GRCh38 (hg38)NC_000009.12Chr92,469,7912,748,000
    nssv18568107RemappedPerfectNC_000009.11:g.246
    9791_2748000del
    GRCh37.p13First PassNC_000009.11Chr92,469,7912,748,000

    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)
    nssv185681074e-061276168
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