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nsv6954921

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 34 studies. See in: genome view    
    Submitted genomic46,212,901-46,220,200Question Mark
    Overlapping variant regions from other studies: 151 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):46,787,036-46,794,335Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6954921Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1346,212,90146,220,200
    nsv6954921RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1346,787,03646,794,335

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18603613duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18603613Submitted genomicNC_000013.11:g.462
    12901_46220200dup
    GRCh38 (hg38)NC_000013.11Chr1346,212,90146,220,200
    nssv18603613RemappedPerfectNC_000013.10:g.467
    87036_46794335dup
    GRCh37.p13First PassNC_000013.10Chr1346,787,03646,794,335

    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)
    nssv186036132.2e-056271972
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