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nsv6858300

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:407

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 19 studies. See in: genome view    
    Submitted genomic83,044,676-83,045,082Question Mark
    Overlapping variant regions from other studies: 84 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):85,659,591-85,659,997Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6858300Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr983,044,67683,045,082
    nsv6858300RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr985,659,59185,659,997

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18746128duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18746128Submitted genomicNC_000009.12:g.830
    44676_83045082dup
    GRCh38 (hg38)NC_000009.12Chr983,044,67683,045,082
    nssv18746128RemappedPerfectNC_000009.11:g.856
    59591_85659997dup
    GRCh37.p13First PassNC_000009.11Chr985,659,59185,659,997

    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)
    nssv187461288e-062243940
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