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nsv7039581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94,835

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 355 SVs from 47 studies. See in: genome view    
    Submitted genomic40,471,473-40,566,307Question Mark
    Overlapping variant regions from other studies: 355 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):40,698,613-40,793,447Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039581Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr240,471,47340,566,307
    nsv7039581RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr240,698,61340,793,447

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769172inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769172Submitted genomicNC_000002.12:g.404
    71473_40566307inv
    GRCh38 (hg38)NC_000002.12Chr240,471,47340,566,307
    nssv18769172RemappedPerfectNC_000002.11:g.406
    98613_40793447inv
    GRCh37.p13First PassNC_000002.11Chr240,698,61340,793,447

    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)
    nssv187691724e-061276268
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