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nsv6787299

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,482

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view    
    Submitted genomic138,209,655-138,212,136Question Mark
    Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):137,545,344-137,547,825Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6787299Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5138,209,655138,212,136
    nsv6787299RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5137,545,344137,547,825

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18699743duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18699743Submitted genomicNC_000005.10:g.138
    209655_138212136du
    p
    GRCh38 (hg38)NC_000005.10Chr5138,209,655138,212,136
    nssv18699743RemappedPerfectNC_000005.9:g.1375
    45344_137547825dup
    GRCh37.p13First PassNC_000005.9Chr5137,545,344137,547,825

    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)
    nssv186997432.5e-057272408
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