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nsv6665900

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,129,126

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6023 SVs from 119 studies. See in: genome view    
    Submitted genomic247,656,440-248,785,565Question Mark
    Overlapping variant regions from other studies: 5623 SVs from 119 studies. See in: genome view    
    Remapped(Score: Pass):247,819,742-248,865,778Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6665900Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1247,656,440248,785,565
    nsv6665900RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1247,819,742248,865,778

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609870duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609870Submitted genomicNC_000001.11:g.247
    656440_248785565du
    p
    GRCh38 (hg38)NC_000001.11Chr1247,656,440248,785,565
    nssv18609870RemappedPassNC_000001.10:g.247
    819742_248865778du
    p
    GRCh37.p13First PassNC_000001.10Chr1247,819,742248,865,778

    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)
    nssv186098703.2e-059271370
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