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nsv6859905

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:156

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 17 studies. See in: genome view    
    Submitted genomic93,482,308-93,482,463Question Mark
    Overlapping variant regions from other studies: 86 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):96,244,590-96,244,745Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6859905Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr993,482,30893,482,463
    nsv6859905RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr996,244,59096,244,745

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749635duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749635Submitted genomicNC_000009.12:g.934
    82308_93482463dup
    GRCh38 (hg38)NC_000009.12Chr993,482,30893,482,463
    nssv18749635RemappedPerfectNC_000009.11:g.962
    44590_96244745dup
    GRCh37.p13First PassNC_000009.11Chr996,244,59096,244,745

    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)
    nssv187496359e-062225316
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