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nsv6861987

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:979,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2498 SVs from 91 studies. See in: genome view    
    Submitted genomic12,898,301-13,877,400Question Mark
    Overlapping variant regions from other studies: 2503 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):12,898,300-13,877,399Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6861987Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr912,898,30113,877,400
    nsv6861987RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr912,898,30013,877,399

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749963duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749963Submitted genomicNC_000009.12:g.128
    98301_13877400dup
    GRCh38 (hg38)NC_000009.12Chr912,898,30113,877,400
    nssv18749963RemappedPerfectNC_000009.11:g.128
    98300_13877399dup
    GRCh37.p13First PassNC_000009.11Chr912,898,30013,877,399

    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)
    nssv18749963<0.00156217120
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