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nsv7048784

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:817,304

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2082 SVs from 93 studies. See in: genome view    
    Submitted genomic231,275,843-232,093,146Question Mark
    Overlapping variant regions from other studies: 2085 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):231,411,589-232,228,892Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048784Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,275,843232,093,146
    nsv7048784RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,411,589232,228,892

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758654inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758654Submitted genomicNC_000001.11:g.231
    275843_232093146in
    v
    GRCh38 (hg38)NC_000001.11Chr1231,275,843232,093,146
    nssv18758654RemappedPerfectNC_000001.10:g.231
    411589_232228892in
    v
    GRCh37.p13First PassNC_000001.10Chr1231,411,589232,228,892

    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)
    nssv187586541.4e-054274318
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