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nsv7028188

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,273,994

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5088 SVs from 88 studies. See in: genome view    
    Submitted genomic48,271,055-52,545,048Question Mark
    Overlapping variant regions from other studies: 926 SVs from 31 studies. See in: genome view    
    Remapped(Score: Pass):1-2,258,163Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7028188Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX48,271,05552,545,048
    nsv7028188RemappedPassGRCh37.p13PATCHESFirst PassNW_004070877.1ChrX|NW_00
    4070877.1
    12,258,163

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766948inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766948Submitted genomicNC_000023.11:g.482
    71055_52545048inv
    GRCh38 (hg38)NC_000023.11ChrX48,271,05552,545,048
    nssv18766948RemappedPassNW_004070877.1:g.1
    _2258163inv
    GRCh37.p13First PassNW_004070877.1ChrX|NW_00
    4070877.1
    12,258,163

    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)
    nssv187669485e-061200000
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