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nsv6969131

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,074,413

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 21778 SVs from 138 studies. See in: genome view    
    Submitted genomic22,744,959-28,819,371Question Mark
    Overlapping variant regions from other studies: 19050 SVs from 135 studies. See in: genome view    
    Remapped(Score: Pass):23,564,855-29,064,517Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6969131Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1522,744,95928,819,371
    nsv6969131RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1523,564,85529,064,517

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18393270deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18393270Submitted genomicNC_000015.10:g.227
    44959_28819371del
    GRCh38 (hg38)NC_000015.10Chr1522,744,95928,819,371
    nssv18393270RemappedPassNC_000015.9:g.2356
    4855_29064517del
    GRCh37.p13First PassNC_000015.9Chr1523,564,85529,064,517

    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)
    nssv183932704e-061256296
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