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nsv6771238

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:539

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 75 SVs from 12 studies. See in: genome view    
    Submitted genomic73,496,929-73,497,467Question Mark
    Overlapping variant regions from other studies: 75 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):72,792,754-72,793,292Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6771238Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr573,496,92973,497,467
    nsv6771238RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr572,792,75472,793,292

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18705459duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18705459Submitted genomicNC_000005.10:g.734
    96929_73497467dup
    GRCh38 (hg38)NC_000005.10Chr573,496,92973,497,467
    nssv18705459RemappedPerfectNC_000005.9:g.7279
    2754_72793292dup
    GRCh37.p13First PassNC_000005.9Chr572,792,75472,793,292

    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)
    nssv187054594e-061244458
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