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nsv6716373

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:281

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 24 studies. See in: genome view    
    Submitted genomic55,069,796-55,070,076Question Mark
    Overlapping variant regions from other studies: 91 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):55,103,823-55,104,103Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6716373Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr355,069,79655,070,076
    nsv6716373RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr355,103,82355,104,103

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18678432duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18678432Submitted genomicNC_000003.12:g.550
    69796_55070076dup
    GRCh38 (hg38)NC_000003.12Chr355,069,79655,070,076
    nssv18678432RemappedPerfectNC_000003.11:g.551
    03823_55104103dup
    GRCh37.p13First PassNC_000003.11Chr355,103,82355,104,103

    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)
    nssv186784324e-061234108
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