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nsv7051654

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,787,432

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5851 SVs from 111 studies. See in: genome view    
    Submitted genomic109,433,715-112,221,146Question Mark
    Overlapping variant regions from other studies: 5855 SVs from 111 studies. See in: genome view    
    Remapped(Score: Perfect):108,769,416-111,556,843Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051654Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5109,433,715112,221,146
    nsv7051654RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5108,769,416111,556,843

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774401inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774401Submitted genomicNC_000005.10:g.109
    433715_112221146in
    v
    GRCh38 (hg38)NC_000005.10Chr5109,433,715112,221,146
    nssv18774401RemappedPerfectNC_000005.9:g.1087
    69416_111556843inv
    GRCh37.p13First PassNC_000005.9Chr5108,769,416111,556,843

    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)
    nssv187744014e-061276268
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