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nsv6671381

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 215 SVs from 28 studies. See in: genome view    
    Submitted genomic246,878,401-246,882,700Question Mark
    Overlapping variant regions from other studies: 218 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):247,041,703-247,046,002Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6671381Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1246,878,401246,882,700
    nsv6671381RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1247,041,703247,046,002

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609822duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609822Submitted genomicNC_000001.11:g.246
    878401_246882700du
    p
    GRCh38 (hg38)NC_000001.11Chr1246,878,401246,882,700
    nssv18609822RemappedPerfectNC_000001.10:g.247
    041703_247046002du
    p
    GRCh37.p13First PassNC_000001.10Chr1247,041,703247,046,002

    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)
    nssv186098224e-061274138
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